US8809264B2

Quinoxalinyl macrocyclic hepatitis C virus serine protease inhibitors

Claim Score by NHIP

Abstract

The present invention relates to compounds, including compounds of Formula I, or a pharmaceutically acceptable salt, ester, or prodrug, thereof: which inhibit serine protease activity, particularly the activity of hepatitis C virus (HCV) NS3-NS4A protease. Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.

US8809264B2, drawing sheet 1 — Sheet 1 of 834

Term

Projected expiry 2 March 2029.

15 claims: 5 independent, 10 dependent

1
A compound of Formula I:as well as the pharmaceutically acceptable salts thereof, wherein: A is selected from H, —(C═O)—O—R 1 , —(C═O)—R 2 , —C(═O)—NH—R 2 , or —S(O) 2 —R 1 , —S(O) 2 NHR 2 ;each R 1 is independently selected from the group consisting of: (i) aryl;substituted aryl;heteroaryl;substituted heteroaryl;(ii) heterocycloalkyl or substituted heterocycloalkyl;(iii) —C 1 -C 8 alkyl, —C 2 -C 8 alkenyl, or —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N;substituted —C 1 -C 8 alkyl, substituted —C 2 -C 8 alkenyl, or substituted —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N;—C 3 -C 12 cycloalkyl, or substituted —C 3 -C 12 cycloalkyl;—C 3 -C 12 cycloalkenyl, or substituted —C 3 -C 12 cycloalkenyl;each R 2 is independently selected from the group consisting of: (i) hydrogen;(ii) aryl;substituted aryl;heteroaryl;substituted heteroaryl;(iii) heterocycloalkyl or substituted heterocycloalkyl;(iv) —C 1 -C 8 alkyl, —C 2 -C 8 alkenyl, or —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N;substituted —C 1 -C 8 alkyl, substituted —C 2 -C 8 alkenyl, or substituted —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N;—C 3 -C 12 cycloalkyl, or substituted —C 3 -C 12 cycloalkyl;—C 3 -C 12 cycloalkenyl, or substituted —C 3 -C 12 cycloalkenyl;G is selected from-NHS(O) 2 —R 3 ;where each R 3 is independently selected from: (i) heterocycloalkyl or substituted heterocycloalkyl;and (ii) C 3 -C 12 cycloalkyl, or substituted —C 3 -C 12 cycloalkyl;—C 3 -C 12 cycloalkenyl, or substituted —C 3 -C 12 cycloalkenyl;L is selected from —CH 2 —, —O—, —S—, or —S(O) 2 —;X and Y taken together with the carbon atoms to which they are attached to form a cyclic moiety selected from aryl, substituted aryl, heteroaryl, or substituted heteroaryl;W is absent;Z is selected from the groups consisting of: (vi) aryl, substituted aryl;(vii) heteroaryl, substituted heteroaryl;(viii) —C 3 -C 12 cycloalkyl, substituted —C 3 -C 12 cycloalkyl, heterocycloalkyl, substituted heterocycloalkyl;(ix) —C 1 -C 6 alkyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;(x) —C 2 -C 6 alkenyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;(xi) —C 2 -C 6 alkynyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;j=0, 1, 2, 3, or 4;k=1, 2, or 3;m=0, 1, or 2;and denotes a carbon-carbon single or double bond.
2
A compound of Formula II:as well as the pharmaceutically acceptable salts thereof, wherein each of X 1 , X 2 , X 3 and X 4 are independently selected from —CR 6 and N, wherein R 6 is independently selected from: (i) hydrogen;halogen;—NO 2 ;—CN;(ii) -M-R 4 , M is O, S, NH, where R 4 is as previously defined;(iii) NR 4 R 5 , where R 4 and R 5 are as previously defined;(iv) —C 1 -C 8 alkyl, —C 2 -C 8 alkenyl, or —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N;substituted —C 1 -C 8 alkyl, substituted —C 2 -C 8 alkenyl, or substituted —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N;—C 3 -C 12 cycloalkyl, or substituted —C 3 -C 12 cycloalkyl;—C 3 -C 12 cycloalkenyl, or substituted —C 3 -C 12 cycloalkenyl;(v) aryl;substituted aryl;heteroaryl;substituted heteroaryl;(vi) heterocycloalkyl or substituted heterocycloalkyl;A is selected from H, —(C═O)—O—R 1 , —(C═O)—R 2 , —C(═O)—NH—R 2 , or —S(O) 2 —R 1 , —S(O) 2 NHR 2 ;each R 1 is independently selected from the group consisting of: (i) aryl;substituted aryl;heteroaryl;substituted heteroaryl;(ii) heterocycloalkyl or substituted heterocycloalkyl;(iii) —C 1 -C 8 alkyl, —C 2 -C 8 alkenyl, or —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N;substituted —C 1 -C 8 alkyl, substituted —C 2 -C 8 alkenyl, or substituted —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N;—C 3 -C 12 cycloalkyl, or substituted —C 3 -C 12 cycloalkyl;—C 3 -C 12 cycloalkenyl, or substituted —C 3 -C 12 cycloalkenyl;each R 2 is independently selected from the group consisting of: (i) hydrogen;(ii) aryl;substituted aryl;heteroaryl;substituted heteroaryl;(iii) heterocycloalkyl or substituted heterocycloalkyl;(iv) —C 1 -C 8 alkyl, —C 2 -C 8 alkenyl, or —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N;substituted —C 1 -C 8 alkyl, substituted —C 2 -C 8 alkenyl, or substituted —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N;—C 3 -C 12 cycloalkyl, or substituted —C 3 -C 12 cycloalkyl;—C 3 -C 12 cycloalkenyl, or substituted —C 3 -C 12 cycloalkenyl;G is selected from —NHS(O) 2 —R 3 ;where each R 3 is independently selected from: (i) heterocycloalkyl or substituted heterocycloalkyl;and (ii) C 3 -C 12 cycloalkyl, or substituted —C 3 -C 12 cycloalkyl;—C 3 -C 12 cycloalkenyl, or substituted —C 3 -C 12 cycloalkenyl;W is absent;Z is selected from the groups consisting of: (vi) aryl, substituted aryl;(vii) heteroaryl, substituted heteroaryl;(viii) —C 3 -C 12 cycloalkyl, substituted —C 3 -C 12 cycloalkyl, heterocycloalkyl, substituted heterocycloalkyl;(ix) —C 1 -C 6 alkyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;(x) —C 2 -C 6 alkenyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;or (xi) —C 2 -C 6 alkynyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl.
5
A compound of Formula III:as well as the pharmaceutically acceptable salts thereof, wherein: each of Y 1 , Y 2 and Y 3 are independently selected from CR 6 , N, NR 6 , S and O;A is selected from H, —(C═O)—O—R 1 , —(C═O)—R 2 , —C(═O)—NH—R 2 , or —S(O) 2 —R 1 , —S(O) 2 NHR 2 ;each R 1 is independently selected from the group consisting of: (i) aryl;substituted aryl;heteroaryl;substituted heteroaryl;(ii) heterocycloalkyl or substituted heterocycloalkyl;(iii) —C 1 -C 8 alkyl, —C 2 -C 8 alkenyl, or —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N;substituted —C 1 -C 8 alkyl, substituted —C 2 -C 8 alkenyl, or substituted —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N;—C 3 -C 12 cycloalkyl, or substituted —C 3 -C 12 cycloalkyl;—C 3 -C 12 cycloalkenyl, or substituted —C 3 -C 12 cycloalkenyl;each R 2 is independently selected from the group consisting of: (i) hydrogen;(ii) aryl;substituted aryl;heteroaryl;substituted heteroaryl;(iii) heterocycloalkyl or substituted heterocycloalkyl;(iv) —C 1 -C 8 alkyl, —C 2 -C 8 alkenyl, or —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N;substituted —C 1 -C 8 alkyl, substituted —C 2 -C 8 alkenyl, or substituted —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N;—C 3 -C 12 cycloalkyl, or substituted —C 3 -C 12 cycloalkyl;—C 3 -C 12 cycloalkenyl, or substituted —C 3 -C 12 cycloalkenyl;G is selected from —NHS(O) 2 —R 3 ;where each R 3 is independently selected from: (i) heterocycloalkyl or substituted heterocycloalkyl;and C 3 -C 12 cycloalkyl, or substituted —C 3 -C 12 cycloalkyl;—C 3 -C 12 cycloalkenyl, or substituted —C 3 -C 12 cycloalkenyl;W is absent;Z is selected from the groups consisting of: (vi) aryl, substituted aryl;(vii) heteroaryl, substituted heteroaryl;(viii) —C 3 -C 12 cycloalkyl, substituted —C 3 -C 12 cycloalkyl, heterocycloalkyl, substituted heterocycloalkyl;(ix) —C 1 -C 6 alkyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;(x) —C 2 -C 6 alkenyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;—C 2 -C 6 alkynyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;and R 6 is independently selected from: (i) hydrogen;halogen;—NO 2 ;—CN;(ii) -M-R 4 , M is O, S, NH, where R 4 is as previously defined;(iii) NR 4 R 5 , where R 4 and R 5 are as previously defined;(iv) —C 1 -C 8 alkyl, —C 2 -C 8 alkenyl, or —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N;substituted —C 1 -C 8 alkyl, substituted —C 2 -C 8 alkenyl, or substituted —C 2 -C 8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N;—C 3 -C 12 cycloalkyl, or substituted —C 3 -C 12 cycloalkyl;—C 3 -C 12 cycloalkenyl, or substituted —C 3 -C 12 cycloalkenyl;(v) aryl;substituted aryl;heteroaryl;substituted heteroaryl;(vi) heterocycloalkyl or substituted heterocycloalkyl.
8
A compound which is selected from compounds of Formula IV, where A, Q and G are delineated in Table 1:TABLE 1 (IV) Example # I. A II. Q G 46 47 48 49 50 51 52 —H 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 69 70 74 75 76 77 78 79 80 81 82 83 84 85 86 88 89 90 91 92 93 94 95 96 97 98 99 101 102 103 104 105 106 107 108 109 110 111
9
Broadest claimClaim Score 89, very broad(NHIP)A compound represented by Formula IV:or a pharmaceutically acceptable salt thereof, wherein A is selected from Table 2, Q is selected from Table 3, G is selected from Table 4: TABLE 2 A-Matrix TABLE 3 Q-Matrix TABLE 4 G-Matrix

Independent claims5

567 paragraphs in 6 sections, as filed

This application claims the benefit of U.S. Provisional Application No. 60/872,442, filed on Jun. 26, 2006. The entire teachings of the above applications are incorporated herein by reference.

TECHNICAL FIELD

The present invention relates to novel macrocycles having activity against the hepatitis C virus (HCV) and useful in the treatment of HCV infections. More particularly, the invention relates to macrocyclic compounds, compositions containing such compounds and methods for using the same, as well as processes for making such compounds.

BACKGROUND OF THE INVENTION

HCV is the principal cause of non-A, non-B hepatitis and is an increasingly severe public health problem both in the developed and developing world. It is estimated that the virus infects over 200 million people worldwide, surpassing the number of individuals infected with the human immunodeficiency virus (HIV) by nearly five fold. HCV infected patients, due to the high percentage of individuals inflicted with chronic infections, are at an elevated risk of developing cirrhosis of the liver, subsequent hepatocellular carcinoma and terminal liver disease. HCV is the most prevalent cause of hepatocellular cancer and cause of patients requiring liver transplantations in the western world.

There are considerable barriers to the development of anti-HCV therapeutics, which include, but are not limited to, the persistence of the virus, the genetic diversity of the virus during replication in the host, the high incident rate of the virus developing drug-resistant mutants, and the lack of reproducible infectious culture systems and small-animal models for HCV replication and pathogenesis. In a majority of cases, given the mild course of the infection and the complex biology of the liver, careful consideration must be given to antiviral drugs, which are likely to have significant side effects.

Only two approved therapies for HCV infection are currently available. The original treatment regimen generally involves a 3-12 month course of intravenous interferon-α (IFN-α), while a new approved second-generation treatment involves co-treatment with IFN-α and the general antiviral nucleoside mimics like ribavirin. Both of these treatments suffer from interferon related side effects as well as low efficacy against HCV infections. There exists a need for the development of effective antiviral agents for treatment of HCV infection due to the poor tolerability and disappointing efficacy of existing therapies.

In a patient population where the majority of individuals are chronically infected and asymptomatic and the prognoses are unknown, an effective drug preferably possesses significantly fewer side effects than the currently available treatments. The hepatitis C non-structural protein-3 (NS3) is a proteolytic enzyme required for processing of the viral polyprotein and consequently viral replication. Despite the huge number of viral variants associated with HCV infection, the active site of the NS3 protease remains highly conserved thus making its inhibition an attractive mode of intervention. Recent success in the treatment of HIV with protease inhibitors supports the concept that the inhibition of NS3 is a key target in the battle against HCV.

HCV is a flaviridae type RNA virus. The HCV genome is enveloped and contains a single strand RNA molecule composed of circa 9600 base pairs. It encodes a polypeptide comprised of approximately 3010 amino acids.

The HCV polyprotein is processed by viral and host peptidase into 10 discreet peptides which serve a variety of functions. There are three structural proteins, C, E1 and E2. The P7 protein is of unknown function and is comprised of a highly variable sequence. There are six non-structural proteins. NS2 is a zinc-dependent metalloproteinase that functions in conjunction with a portion of the NS3 protein. NS3 incorporates two catalytic functions (separate from its association with NS2): a serine protease at the N-terminal end, which requires NS4A as a cofactor, and an ATP-ase-dependent helicase function at the carboxyl terminus. NS4A is a tightly associated but non-covalent cofactor of the serine protease.

The NS3.4A protease is responsible for cleaving four sites on the viral polyprotein. The NS3-NS4A cleavage is autocatalytic, occurring in cis. The remaining three hydrolyses, NS4A-NS4B, NS4B-NS5A and NS5A-NS5B all occur in trans. NS3 is a serine protease which is structurally classified as a chymotrypsin-like protease. While the NS serine protease possesses proteolytic activity by itself, the HCV protease enzyme is not an efficient enzyme in terms of catalyzing polyprotein cleavage. It has been shown that a central hydrophobic region of the NS4A protein is required for this enhancement. The complex formation of the NS3 protein with NS4A seems necessary to the processing events, enhancing the proteolytic efficacy at all of the sites.

A general strategy for the development of antiviral agents is to inactivate virally encoded enzymes, including NS3, that are essential for the replication of the virus. Current efforts directed toward the discovery of NS3 protease inhibitors were reviewed by S. Tan, A. Pause, Y. Shi, N. Sonenberg, Hepatitis C Therapeutics: Current Status and Emerging Strategies, Nature Rev. Drug Discov., 1, 867-881 (2002). Other patent disclosures describing the synthesis of HCV protease inhibitors are: WO 00/59929 (2000); WO 99/07733 (1999); WO 00/09543 (2000); WO 99/50230 (1999); U.S. Pat. No. 5,861,297 (1999); U.S. Pat. No. 6,410,531; U.S. Pat. No. 7,176,208; U.S. Pat. No. 7,125,845; US publications 20050153877, and 20050261200.

SUMMARY OF THE INVENTION

The present invention relates to novel HCV protease inhibitor compounds, and pharmaceutically acceptable salts, esters, or prodrugs thereof, which inhibit serine protease activity, particularly the activity of hepatitis C virus (HCV) NS3-NS4A protease. Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds, salts, esters or prodrugs for administration to a subject suffering from HCV infection. The present invention further features pharmaceutical compositions comprising a compound of the present invention (or a pharmaceutically acceptable salt, ester or prodrug thereof) and another anti-HCV agent, such as interferon (e.g., alpha-interferon, beta-interferon, consensus interferon, pegylated interferon, or albumin or other conjugated interferon), ribavirin, amantadine, another HCV protease inhibitor, or an HCV polymerase, helicase or internal ribosome entry site inhibitor. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition of the present invention.

In one embodiment of the present invention there are disclosed compounds represented by Formula I, or pharmaceutically acceptable salts, esters, or prodrugs thereof:

<chemistry id="CHEM-US-00002" num="00002"><img id="EMI-C00002" he="52.66mm" wi="69.85mm" file="US08809264-20140819-C00002.TIF" alt="embedded image" img-content="chem" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00002" attachment-type="cdx" file="US08809264-20140819-C00002.CDX" /><attachment idref="CHEM-US-00002" attachment-type="mol" file="US08809264-20140819-C00002.MOL" /></attachments></chemistry> as well as the pharmaceutically acceptable salts, esters and prodrugs thereof, wherein:

A is selected from H, —(C═O)—O—R1, —(C═O)—R2, —C(═O)—NH—R2, or —S(O)2—R1, —S(O)2NHR2;

each R1 is independently selected from the group consisting of: <ul><li id="ul0001-0001" num="0000"><ul><li id="ul0002-0001" num="0016">(i) aryl; substituted aryl; heteroaryl; substituted heteroaryl;</li><li id="ul0002-0002" num="0017">(ii) heterocycloalkyl or substituted heterocycloalkyl;</li><li id="ul0002-0003" num="0018">(iii) —C1-C8 alkyl, —C2-C8 alkenyl, or —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N; substituted —C1-C8 alkyl, substituted —C2-C8 alkenyl, or substituted —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N; —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkyl; —C3-C12 cycloalkenyl, or substituted —C3-C12 cycloalkenyl;</li></ul></li></ul>

each R2 is independently selected from the group consisting of: <ul><li id="ul0003-0001" num="0000"><ul><li id="ul0004-0001" num="0020">(i) hydrogen;</li><li id="ul0004-0002" num="0021">(ii) aryl; substituted aryl; heteroaryl; substituted heteroaryl;</li><li id="ul0004-0003" num="0022">(iii) heterocycloalkyl or substituted heterocycloalkyl;</li><li id="ul0004-0004" num="0023">(iv) —C1-C8 alkyl, —C2-C8 alkenyl, or —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N; substituted —C1-C8 alkyl, substituted —C2-C8 alkenyl, or substituted —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N; —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkyl; —C3-C12 cycloalkenyl, or substituted —C3-C12 cycloalkenyl;</li></ul></li></ul>

G is —NHS(O)2—R3, where each R3 is independently selected from: <ul><li id="ul0005-0001" num="0000"><ul><li id="ul0006-0001" num="0025">(i) heterocycloalkyl or substituted heterocycloalkyl; and</li><li id="ul0006-0002" num="0026">(ii) —C1-C8 alkyl, —C2-C8 alkenyl, or —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N, substituted —C1-C8 alkyl, substituted —C2-C8 alkenyl, or substituted —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N; —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkyl; —C3-C12 cycloalkenyl, or substituted —C3-C12 cycloalkenyl;</li></ul></li></ul>

with a proviso that R3 is not —CH2Ph or —CH2CH2Ph;

L is selected from —CH2—, —O—, —S—, or —S(O)2—;

X and Y taken together with the carbon atoms to which they are attached to form a cyclic moiety selected from aryl, substituted aryl, heteroaryl, or substituted heteroaryl;

W is absent, or selected from —O—, —S—, —NH—, —N(Me)-, —C(O)NH—, or —C(O)N(Me)-;

alternatively, W can be —C2-C4 alkylene-, substituted —C2-C4 alkylene-;

Z is selected from the groups consisting of: <ul><li id="ul0007-0001" num="0000"><ul><li id="ul0008-0001" num="0033">(i) hydrogen;</li><li id="ul0008-0002" num="0034">(ii) —CN;</li><li id="ul0008-0003" num="0035">(iii) —N3;</li><li id="ul0008-0004" num="0036">(iv) halogen;</li><li id="ul0008-0005" num="0037">(v) —NH—N═CH(R2), where R2 is as previously defined above;</li><li id="ul0008-0006" num="0038">(vi) aryl, substituted aryl;</li><li id="ul0008-0007" num="0039">(vii) heteroaryl, substituted heteroaryl;</li><li id="ul0008-0008" num="0040">(viii) —C3-C12 cycloalkyl, substituted —C3-C12 cycloalkyl, heterocycloalkyl, substituted heterocycloalkyl;</li><li id="ul0008-0009" num="0041">(ix) —C1-C6 alkyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;</li><li id="ul0008-0010" num="0042">(x) —C2-C6 alkenyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;</li><li id="ul0008-0011" num="0043">(xi) —C2-C6 alkynyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;</li></ul></li></ul>

j=0, 1, 2, 3, or 4;

k=1, 2, or 3;

m=0, 1, or 2; and

<img id="CUSTOM-CHARACTER-00001" he="3.13mm" wi="6.35mm" file="US08809264-20140819-P00001.TIF" alt="custom character" img-content="character" img-format="tif" orientation="portrait" inline="no" /> denotes a carbon-carbon single or double bond.

In another embodiment, the present invention features pharmaceutical compositions comprising a compound of the invention, or a pharmaceutically acceptable salt, ester or prodrug thereof. In still another embodiment of the present invention there are disclosed pharmaceutical compositions comprising a therapeutically effective amount of a compound of the invention, or a pharmaceutically acceptable salt, ester or prodrug thereof, in combination with a pharmaceutically acceptable carrier or excipient. In yet another embodiment of the invention are methods of treating a hepatitis C infection in a subject in need of such treatment with said pharmaceutical compositions.

DETAILED DESCRIPTION OF THE INVENTION

A first embodiment of the invention is a compound represented by Formula I as described above, or a pharmaceutically acceptable salt, ester or prodrug thereof, alone or in combination with a pharmaceutically acceptable carrier or excipient.

In other embodiments of the invention are compounds represented by Formulae II-V as described herein, or pharmaceutically acceptable salts, esters or prodrugs thereof, alone or in combination with a pharmaceutically acceptable carrier or excipient.

A compound of Formula II:

wherein each of X1, X2, X3 and X4 are independently selected from —CR6 and N, wherein R6 is independently selected from: <ul><li id="ul0009-0001" num="0000"><ul><li id="ul0010-0001" num="0054">(i) hydrogen; halogen; —NO2; —CN;</li><li id="ul0010-0002" num="0055">(ii) -M-R4, M is O, S, NH, where R4 is as previously defined;</li><li id="ul0010-0003" num="0056">(iii) NR4R5, where R4 and R5 are as previously defined;</li><li id="ul0010-0004" num="0057">(iv) —C1-C8 alkyl, —C2-C8 alkenyl, or —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N; substituted —C1-C8 alkyl, substituted —C2-C8 alkenyl, or substituted —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N; —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkyl; —C3-C12 cycloalkenyl, or substituted —C3-C12 cycloalkenyl;</li><li id="ul0010-0005" num="0058">(v) aryl; substituted aryl; heteroaryl; substituted heteroaryl;</li><li id="ul0010-0006" num="0059">(vi) heterocycloalkyl or substituted heterocycloalkyl;</li></ul></li></ul>

where A, G, W, Z are as defined for Formula I.

In one example, W is absent, —C2-C4 alkylene-, or substituted —C2-C4 alkylene-. Z is heteroaryl, substitute heteroaryl, aryl, or substituted aryl. A is selected from the group consisting of —C(O)—R2, —C(O)—O—R2, —S(O)2NHR2 and —C(O)—NH—R2, where R2 is selected from aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic, —C1-C8 alkyl, —C2-C8 alkenyl, —C2-C8 alkynyl, substituted —C1-C8 alkyl, substituted —C2-C8 alkenyl, substituted —C2-C8 alkynyl, —C3-C12 cycloalkyl, —C3-C12 cycloalkenyl, substituted —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkenyl. G is —NHSO2—R3, where R3 is selected from —C1-C8 alkyl, —C2-C8 alkenyl, —C2-C8 alkynyl, heterocyclic, substituted heterocyclic, —C3-C12 cycloalkyl, —C3-C12 cycloalkenyl, substituted —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkenyl.

In another example, W is absent, —C2-C4 alkylene-, or substituted —C2-C4 alkylene-. Z is heteroaryl, substitute heteroaryl, aryl, or substituted aryl. A is —C(O)—O—R2, —S(O)2NHR2 or —C(O)—NH—R2, where R2 is —C1-C8 alkyl, —C2-C8 alkenyl, —C2-C8 alkynyl, substituted —C1-C8 alkyl, substituted —C2-C8 alkenyl, substituted —C2-C8 alkynyl, —C3-C12 cycloalkyl, —C3-C12 cycloalkenyl, substituted —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkenyl. G is —NHSO2—R3, where R3 is selected from —C1-C8 alkyl, heterocyclic, substituted heterocyclic, —C3-C12 cycloalkyl, —C3-C12 cycloalkenyl, substituted —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkenyl.

In another example, W is absent. Z is heteroaryl, substitute heteroaryl, aryl, or substituted aryl. A is —C(O)—O—R1, where R1 is —C1-C8 alkyl, —C3-C12 cycloalkyl, substituted —C3-C12 cycloalkyl, heteroaryl, or substituted heteroaryl. G is —NHSO2—R3, where R3 is selected from —C3-C12 cycloalkyl or substituted —C3-C12 cycloalkyl.

In a preferred example, W is absent. Z is heteroaryl or substitute heteroaryl. A is —C(O)—O—R1, where R1 is —C1-C8 alkyl, —C3-C12 cycloalkyl, substituted —C3-C12 cycloalkyl, heteroaryl, or substituted heteroaryl. G is —NHSO2—R3, where R3 is selected from —C3-C12 cycloalkyl or substituted —C3-C12 cycloalkyl.

In another preferred example, W is absent. Z is 2-thiophenyl. A is —C(O)—O—R1, where R1 is —C1-C8 alkyl, —C3-C12 cycloalkyl, substituted —C3-C12 cycloalkyl, heteroaryl, or substituted heteroaryl. G is —NHSO2—R3, where R3 is selected from —C3-C12 cycloalkyl or substituted —C3-C12 cycloalkyl.

In still another preferred example, a compound of Formula II has a formula selected from Formulae II′ or II″:

<chemistry id="CHEM-US-00004" num="00004"><img id="EMI-C00004" he="118.87mm" wi="69.85mm" file="US08809264-20140819-C00004.TIF" alt="embedded image" img-content="chem" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00004" attachment-type="cdx" file="US08809264-20140819-C00004.CDX" /><attachment idref="CHEM-US-00004" attachment-type="mol" file="US08809264-20140819-C00004.MOL" /></attachments></chemistry> wherein A is —C(O)—O—R1, and R1 is —C1-C8 alkyl, —C3-C12 cycloalkyl, substituted —C3-C12 cycloalkyl, heterocycloalkyl or substituted heterocycloalkyl. G is —NHSO2—R3, and R3 is selected from —C3-C12 cycloalkyl (e.g., cyclopropyl) or substituted —C3-C12 cycloalkyl. R100 is hydrogen or —O—CH3.

A compound of Formula III:

<chemistry id="CHEM-US-00005" num="00005"><img id="EMI-C00005" he="48.77mm" wi="69.85mm" file="US08809264-20140819-C00005.TIF" alt="embedded image" img-content="chem" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00005" attachment-type="cdx" file="US08809264-20140819-C00005.CDX" /><attachment idref="CHEM-US-00005" attachment-type="mol" file="US08809264-20140819-C00005.MOL" /></attachments></chemistry><ul><li id="ul0011-0001" num="0000"><ul><li id="ul0012-0001" num="0070">wherein each of Y1, Y2, and Y3 is independently selected from CR6, N, NR6, S and O; wherein A, G, W, Z are as defined for Formula I and R6 is as defined for Formula II.</li></ul></li></ul>

In still another example, W is absent, —C2-C4 alkylene-, or substituted —C2-C4 alkylene-. Z is heteroaryl, substitute heteroaryl, aryl, or substituted aryl. A is —C(O)—O—R2, —S(O)2NHR2 or —C(O)—NH—R2, where R2 is —C1-C8 alkyl, —C2-C8 alkenyl, —C2-C8 alkynyl, substituted —C1-C8 alkyl, substituted —C2-C8 alkenyl, substituted —C2-C8 alkynyl, —C3-C12 cycloalkyl, —C3-C12 cycloalkenyl, substituted —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkenyl. G is —NHSO2—R3, where R3 is selected from —C1-C8 alkyl, heterocyclic, substituted heterocyclic, —C3-C12 cycloalkyl, —C3-C12 cycloalkenyl, substituted —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkenyl.

In still yet another example, W is absent. Z is heteroaryl, substitute heteroaryl, aryl, or substituted aryl. A is —C(O)—O—R1, where R1 is —C1-C8 alkyl, —C3-C12 cycloalkyl, substituted —C3-C12 cycloalkyl, heteroaryl, or substituted heteroaryl. G is —NHSO2—R3, where R3 is selected from —C3-C12 cycloalkyl or substituted —C3-C12 cycloalkyl.

In still another example, W is absent. Z is heteroaryl, substitute heteroaryl. A is —C(O)—O—R1, where R1 is —C1-C8 alkyl, —C3-C12 cycloalkyl, substituted —C3-C12 cycloalkyl, heteroaryl, or substituted heteroaryl. G is —NHSO2—R3, where R3 is selected from —C3-C12 cycloalkyl or substituted —C3-C12 cycloalkyl.

In another example, W is absent. Z is 2-thiophenyl. A is —C(O)—O—R1, where R1 is —C1-C8 alkyl, —C3-C12 cycloalkyl, substituted —C3-C12 cycloalkyl, heteroaryl, or substituted heteroaryl. G is —NHSO2—R3, where R3 is selected from —C3-C12 cycloalkyl or substituted —C3-C12 cycloalkyl.

In yet another example, W is absent. Z can be, without limitation, 2-thiophenyl. A is —C(O)—O—R1, where R1 is —C1-C8 alkyl, —C3-C12 cycloalkyl, substituted —C3-C12 cycloalkyl, heterocyclyl, or substituted heterocyclyl. G is —NHSO2—R3, where R3 is selected from —C3-C12 cycloalkyl or substituted —C3-C12 cycloalkyl.

Representative compounds of the invention include, but are not limited to, the following compounds (Table 1) according to Formula IV:

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/></row><row><entry></entry></row></tbody></tgroup><tgroup align="left" colsep="0" rowsep="0" cols="4"><colspec colname="1" colwidth="35pt" align="center" /><colspec colname="2" colwidth="126pt" align="center" /><colspec colname="3" colwidth="133pt" align="center" /><colspec colname="4" colwidth="91pt" align="center" /><tbody valign="top"><row><entry>Example</entry><entry /><entry /><entry /></row><row><entry>#</entry><entry>A</entry><entry>Q</entry><entry>G</entry></row><row><entry namest="1" nameend="4" align="center" rowsep="1" /></row></tbody></tgroup><tgroup align="left" colsep="0" rowsep="0" cols="4"><colspec colname="1" colwidth="35pt" align="char" char="." /><colspec colname="2" colwidth="126pt" align="center" /><colspec colname="3" colwidth="133pt" align="center" /><colspec colname="4" colwidth="91pt" align="center" /><tbody valign="top"><row><entry>46</entry><entry><chemistry id="CHEM-US-00007" num="00007"><img id="EMI-C00007" he="14.39mm" wi="22.61mm" 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/></attachments></chemistry></entry><entry><chemistry id="CHEM-US-00194" num="00194"><img id="EMI-C00194" he="13.80mm" wi="23.37mm" file="US08809264-20140819-C00194.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00194" attachment-type="cdx" file="US08809264-20140819-C00194.CDX" /><attachment idref="CHEM-US-00194" attachment-type="mol" file="US08809264-20140819-C00194.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry>109</entry><entry><chemistry id="CHEM-US-00195" num="00195"><img id="EMI-C00195" he="15.32mm" wi="26.42mm" file="US08809264-20140819-C00195.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00195" attachment-type="cdx" file="US08809264-20140819-C00195.CDX" /><attachment idref="CHEM-US-00195" attachment-type="mol" file="US08809264-20140819-C00195.MOL" 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nameend="4" align="center" rowsep="1" /></row></tbody></tgroup></table></tables>

Additional compounds of the invention are those of Formula IV:

<chemistry id="CHEM-US-00204" num="00204"><img id="EMI-C00204" he="37.51mm" wi="69.85mm" file="US08809264-20140819-C00204.TIF" alt="embedded image" img-content="chem" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00204" attachment-type="cdx" file="US08809264-20140819-C00204.CDX" /><attachment idref="CHEM-US-00204" attachment-type="mol" file="US08809264-20140819-C00204.MOL" /></attachments></chemistry> wherein A, Q and G are as defined in the A-Matrix, Q-Matrix and G-Matrix tables herein (Tables 2-4). The A-Matrix, Q-Matrix and G-Matrix tables below set forth substituents present on the core ring structure shown in formula (IV) which when one A substituent is selected from the A-Matrix, one Q substituent is selected from the Q-Matrix and one G substituent is selected from the G-Matrix, an additional compound of the invention is described. Compounds are formed by selecting any element from the A-Matrix with any element from the Q-matrix with any element from the G-matrix to arrive upon an A, Q, G-substituted macrocycle of formula IV. For example, a compound of Formula IV, wherein A is element A01 from the A-Matrix, Q is element Q01 from the Q-Matrix, and G is element G02 from the G-Matrix is designated by the number A01Q01G02.

Thus, the invention includes compounds of the formula IV and the pharmaceutically acceptable salts thereof, wherein A is any element in the A-Matrix, Q is any element of the Q-Matrix and G is any element of the G-Matrix.

Specific compounds include, but are not limited to, the following: A01Q01G02; A01Q02G02; A01Q03G02; A01Q38G02; A01Q48G02; A01Q49G02; A01Q61G02; A09Q38G02; A30Q48G02; A05Q38G02; A09Q01G02; A09Q02G02; A09Q03G02; A095Q38G02; A09Q48G02; A30Q03G02; A30Q61G02; A01Q38G02; A05Q16G02; A05Q17G02; A05Q25G02; A03Q01G02; A06Q01G02; A16Q01G02

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orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00229" attachment-type="cdx" file="US08809264-20140819-C00229.CDX" /><attachment idref="CHEM-US-00229" attachment-type="mol" file="US08809264-20140819-C00229.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-26</entry><entry><chemistry id="CHEM-US-00230" num="00230"><img id="EMI-C00230" he="17.02mm" wi="21.76mm" file="US08809264-20140819-C00230.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00230" attachment-type="cdx" file="US08809264-20140819-C00230.CDX" /><attachment idref="CHEM-US-00230" attachment-type="mol" file="US08809264-20140819-C00230.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-27</entry><entry><chemistry id="CHEM-US-00231" num="00231"><img id="EMI-C00231" he="18.03mm" wi="22.78mm" file="US08809264-20140819-C00231.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00231" attachment-type="cdx" file="US08809264-20140819-C00231.CDX" /><attachment idref="CHEM-US-00231" attachment-type="mol" file="US08809264-20140819-C00231.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-28</entry><entry><chemistry id="CHEM-US-00232" num="00232"><img id="EMI-C00232" he="14.48mm" wi="27.69mm" file="US08809264-20140819-C00232.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00232" attachment-type="cdx" file="US08809264-20140819-C00232.CDX" /><attachment idref="CHEM-US-00232" attachment-type="mol" file="US08809264-20140819-C00232.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-29</entry><entry><chemistry id="CHEM-US-00233" num="00233"><img id="EMI-C00233" he="14.48mm" wi="22.78mm" file="US08809264-20140819-C00233.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00233" attachment-type="cdx" file="US08809264-20140819-C00233.CDX" /><attachment idref="CHEM-US-00233" attachment-type="mol" file="US08809264-20140819-C00233.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-30</entry><entry><chemistry id="CHEM-US-00234" num="00234"><img id="EMI-C00234" he="14.48mm" wi="28.28mm" file="US08809264-20140819-C00234.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00234" attachment-type="cdx" file="US08809264-20140819-C00234.CDX" /><attachment idref="CHEM-US-00234" attachment-type="mol" file="US08809264-20140819-C00234.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-31</entry><entry><chemistry id="CHEM-US-00235" num="00235"><img id="EMI-C00235" he="14.48mm" wi="30.31mm" file="US08809264-20140819-C00235.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00235" attachment-type="cdx" file="US08809264-20140819-C00235.CDX" /><attachment idref="CHEM-US-00235" attachment-type="mol" file="US08809264-20140819-C00235.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-32</entry><entry><chemistry id="CHEM-US-00236" num="00236"><img id="EMI-C00236" he="14.56mm" wi="35.14mm" file="US08809264-20140819-C00236.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00236" attachment-type="cdx" file="US08809264-20140819-C00236.CDX" /><attachment idref="CHEM-US-00236" attachment-type="mol" file="US08809264-20140819-C00236.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-33</entry><entry><chemistry id="CHEM-US-00237" num="00237"><img id="EMI-C00237" he="14.48mm" wi="30.31mm" file="US08809264-20140819-C00237.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00237" attachment-type="cdx" file="US08809264-20140819-C00237.CDX" /><attachment idref="CHEM-US-00237" attachment-type="mol" file="US08809264-20140819-C00237.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-34</entry><entry><chemistry id="CHEM-US-00238" num="00238"><img id="EMI-C00238" he="18.03mm" wi="23.62mm" file="US08809264-20140819-C00238.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00238" attachment-type="cdx" file="US08809264-20140819-C00238.CDX" /><attachment idref="CHEM-US-00238" attachment-type="mol" file="US08809264-20140819-C00238.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-35</entry><entry><chemistry id="CHEM-US-00239" num="00239"><img id="EMI-C00239" he="16.93mm" wi="21.76mm" file="US08809264-20140819-C00239.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00239" attachment-type="cdx" file="US08809264-20140819-C00239.CDX" /><attachment idref="CHEM-US-00239" attachment-type="mol" file="US08809264-20140819-C00239.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-36</entry><entry><chemistry id="CHEM-US-00240" num="00240"><img id="EMI-C00240" he="16.26mm" wi="22.27mm" file="US08809264-20140819-C00240.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00240" attachment-type="cdx" file="US08809264-20140819-C00240.CDX" /><attachment idref="CHEM-US-00240" attachment-type="mol" file="US08809264-20140819-C00240.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-37</entry><entry><chemistry id="CHEM-US-00241" num="00241"><img id="EMI-C00241" he="17.86mm" wi="24.21mm" file="US08809264-20140819-C00241.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00241" attachment-type="cdx" file="US08809264-20140819-C00241.CDX" /><attachment idref="CHEM-US-00241" attachment-type="mol" file="US08809264-20140819-C00241.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-38</entry><entry><chemistry id="CHEM-US-00242" num="00242"><img id="EMI-C00242" he="21.84mm" wi="24.21mm" file="US08809264-20140819-C00242.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00242" attachment-type="cdx" file="US08809264-20140819-C00242.CDX" /><attachment idref="CHEM-US-00242" attachment-type="mol" file="US08809264-20140819-C00242.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-39</entry><entry><chemistry id="CHEM-US-00243" num="00243"><img id="EMI-C00243" he="17.02mm" wi="22.52mm" file="US08809264-20140819-C00243.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00243" attachment-type="cdx" file="US08809264-20140819-C00243.CDX" /><attachment idref="CHEM-US-00243" attachment-type="mol" file="US08809264-20140819-C00243.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-40</entry><entry><chemistry id="CHEM-US-00244" num="00244"><img id="EMI-C00244" he="17.02mm" wi="21.76mm" file="US08809264-20140819-C00244.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00244" attachment-type="cdx" file="US08809264-20140819-C00244.CDX" /><attachment idref="CHEM-US-00244" attachment-type="mol" file="US08809264-20140819-C00244.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-41</entry><entry><chemistry id="CHEM-US-00245" num="00245"><img id="EMI-C00245" he="18.03mm" wi="21.76mm" file="US08809264-20140819-C00245.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00245" attachment-type="cdx" file="US08809264-20140819-C00245.CDX" /><attachment idref="CHEM-US-00245" attachment-type="mol" file="US08809264-20140819-C00245.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-42</entry><entry><chemistry id="CHEM-US-00246" num="00246"><img id="EMI-C00246" he="19.22mm" wi="26.59mm" file="US08809264-20140819-C00246.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00246" attachment-type="cdx" file="US08809264-20140819-C00246.CDX" /><attachment idref="CHEM-US-00246" attachment-type="mol" file="US08809264-20140819-C00246.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-43</entry><entry><chemistry id="CHEM-US-00247" num="00247"><img id="EMI-C00247" he="18.03mm" wi="23.54mm" file="US08809264-20140819-C00247.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00247" attachment-type="cdx" file="US08809264-20140819-C00247.CDX" /><attachment idref="CHEM-US-00247" attachment-type="mol" file="US08809264-20140819-C00247.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-44</entry><entry><chemistry id="CHEM-US-00248" num="00248"><img id="EMI-C00248" he="14.48mm" wi="22.78mm" file="US08809264-20140819-C00248.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00248" attachment-type="cdx" file="US08809264-20140819-C00248.CDX" /><attachment idref="CHEM-US-00248" attachment-type="mol" file="US08809264-20140819-C00248.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>A-45</entry><entry><chemistry id="CHEM-US-00249" num="00249"><img id="EMI-C00249" he="29.29mm" wi="29.29mm" file="US08809264-20140819-C00249.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00249" attachment-type="cdx" file="US08809264-20140819-C00249.CDX" /><attachment idref="CHEM-US-00249" attachment-type="mol" file="US08809264-20140819-C00249.MOL" /></attachments></chemistry></entry></row><row><entry namest="1" nameend="3" align="center" rowsep="1" /></row></tbody></tgroup></table></tables>

<tables id="TABLE-US-00003" num="00003"><table frame="none" colsep="0" rowsep="0"><tgroup align="left" colsep="0" rowsep="0" cols="1"><colspec colname="1" colwidth="217pt" align="center" /><thead><row><entry namest="1" nameend="1" rowsep="1">TABLE 3</entry></row><row><entry namest="1" nameend="1" align="center" rowsep="1" /></row><row><entry>Q-Matrix</entry></row><row><entry namest="1" nameend="1" align="center" rowsep="1" /></row></thead><tbody valign="top"><row><entry /></row></tbody></tgroup><tgroup align="left" colsep="0" rowsep="0" cols="3"><colspec colname="1" colwidth="14pt" align="left" /><colspec colname="2" colwidth="21pt" align="center" /><colspec colname="3" colwidth="182pt" align="center" /><tbody valign="top"><row><entry /><entry>Q-01</entry><entry><chemistry id="CHEM-US-00250" num="00250"><img id="EMI-C00250" he="30.14mm" wi="33.44mm" file="US08809264-20140819-C00250.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00250" attachment-type="cdx" file="US08809264-20140819-C00250.CDX" /><attachment idref="CHEM-US-00250" attachment-type="mol" file="US08809264-20140819-C00250.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-02</entry><entry><chemistry id="CHEM-US-00251" num="00251"><img id="EMI-C00251" he="30.14mm" wi="42.42mm" file="US08809264-20140819-C00251.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00251" attachment-type="cdx" file="US08809264-20140819-C00251.CDX" /><attachment idref="CHEM-US-00251" attachment-type="mol" file="US08809264-20140819-C00251.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-03</entry><entry><chemistry id="CHEM-US-00252" num="00252"><img id="EMI-C00252" he="30.14mm" wi="42.42mm" file="US08809264-20140819-C00252.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00252" attachment-type="cdx" file="US08809264-20140819-C00252.CDX" /><attachment idref="CHEM-US-00252" attachment-type="mol" file="US08809264-20140819-C00252.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-04</entry><entry><chemistry id="CHEM-US-00253" num="00253"><img id="EMI-C00253" he="30.14mm" wi="42.08mm" file="US08809264-20140819-C00253.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00253" attachment-type="cdx" file="US08809264-20140819-C00253.CDX" /><attachment idref="CHEM-US-00253" attachment-type="mol" file="US08809264-20140819-C00253.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-05</entry><entry><chemistry id="CHEM-US-00254" num="00254"><img id="EMI-C00254" he="28.87mm" wi="30.31mm" file="US08809264-20140819-C00254.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00254" attachment-type="cdx" file="US08809264-20140819-C00254.CDX" /><attachment idref="CHEM-US-00254" attachment-type="mol" file="US08809264-20140819-C00254.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-06</entry><entry><chemistry id="CHEM-US-00255" num="00255"><img id="EMI-C00255" he="34.29mm" wi="51.82mm" file="US08809264-20140819-C00255.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00255" attachment-type="cdx" file="US08809264-20140819-C00255.CDX" /><attachment idref="CHEM-US-00255" attachment-type="mol" file="US08809264-20140819-C00255.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-07</entry><entry><chemistry id="CHEM-US-00256" num="00256"><img id="EMI-C00256" he="34.37mm" wi="42.08mm" file="US08809264-20140819-C00256.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00256" attachment-type="cdx" file="US08809264-20140819-C00256.CDX" /><attachment idref="CHEM-US-00256" attachment-type="mol" file="US08809264-20140819-C00256.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-08</entry><entry><chemistry id="CHEM-US-00257" num="00257"><img id="EMI-C00257" he="37.00mm" wi="37.08mm" file="US08809264-20140819-C00257.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00257" attachment-type="cdx" file="US08809264-20140819-C00257.CDX" /><attachment idref="CHEM-US-00257" attachment-type="mol" file="US08809264-20140819-C00257.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-09</entry><entry><chemistry id="CHEM-US-00258" num="00258"><img id="EMI-C00258" he="37.00mm" wi="40.98mm" file="US08809264-20140819-C00258.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00258" attachment-type="cdx" file="US08809264-20140819-C00258.CDX" /><attachment idref="CHEM-US-00258" attachment-type="mol" file="US08809264-20140819-C00258.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-10</entry><entry><chemistry id="CHEM-US-00259" num="00259"><img id="EMI-C00259" he="34.97mm" wi="33.44mm" file="US08809264-20140819-C00259.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00259" attachment-type="cdx" file="US08809264-20140819-C00259.CDX" /><attachment idref="CHEM-US-00259" attachment-type="mol" file="US08809264-20140819-C00259.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-11</entry><entry><chemistry id="CHEM-US-00260" num="00260"><img id="EMI-C00260" he="35.81mm" wi="34.54mm" file="US08809264-20140819-C00260.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00260" attachment-type="cdx" file="US08809264-20140819-C00260.CDX" /><attachment idref="CHEM-US-00260" attachment-type="mol" file="US08809264-20140819-C00260.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-12</entry><entry><chemistry id="CHEM-US-00261" num="00261"><img id="EMI-C00261" he="30.14mm" wi="33.44mm" file="US08809264-20140819-C00261.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00261" attachment-type="cdx" file="US08809264-20140819-C00261.CDX" /><attachment idref="CHEM-US-00261" attachment-type="mol" file="US08809264-20140819-C00261.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-13</entry><entry><chemistry id="CHEM-US-00262" num="00262"><img id="EMI-C00262" he="30.14mm" wi="46.99mm" file="US08809264-20140819-C00262.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00262" attachment-type="cdx" file="US08809264-20140819-C00262.CDX" /><attachment idref="CHEM-US-00262" attachment-type="mol" file="US08809264-20140819-C00262.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-14</entry><entry><chemistry id="CHEM-US-00263" num="00263"><img id="EMI-C00263" he="30.14mm" wi="47.58mm" file="US08809264-20140819-C00263.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00263" attachment-type="cdx" file="US08809264-20140819-C00263.CDX" /><attachment idref="CHEM-US-00263" attachment-type="mol" file="US08809264-20140819-C00263.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-15</entry><entry><chemistry id="CHEM-US-00264" num="00264"><img id="EMI-C00264" he="35.48mm" wi="39.37mm" file="US08809264-20140819-C00264.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00264" attachment-type="cdx" file="US08809264-20140819-C00264.CDX" /><attachment idref="CHEM-US-00264" attachment-type="mol" file="US08809264-20140819-C00264.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-16</entry><entry><chemistry id="CHEM-US-00265" num="00265"><img id="EMI-C00265" he="33.44mm" wi="48.26mm" file="US08809264-20140819-C00265.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00265" attachment-type="cdx" file="US08809264-20140819-C00265.CDX" /><attachment idref="CHEM-US-00265" attachment-type="mol" file="US08809264-20140819-C00265.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-17</entry><entry><chemistry id="CHEM-US-00266" num="00266"><img id="EMI-C00266" he="30.99mm" wi="34.71mm" file="US08809264-20140819-C00266.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00266" attachment-type="cdx" file="US08809264-20140819-C00266.CDX" /><attachment idref="CHEM-US-00266" attachment-type="mol" file="US08809264-20140819-C00266.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-18</entry><entry><chemistry id="CHEM-US-00267" num="00267"><img id="EMI-C00267" he="37.00mm" wi="40.98mm" file="US08809264-20140819-C00267.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00267" attachment-type="cdx" file="US08809264-20140819-C00267.CDX" /><attachment idref="CHEM-US-00267" attachment-type="mol" file="US08809264-20140819-C00267.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-19</entry><entry><chemistry id="CHEM-US-00268" num="00268"><img id="EMI-C00268" he="37.00mm" wi="40.98mm" file="US08809264-20140819-C00268.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00268" attachment-type="cdx" file="US08809264-20140819-C00268.CDX" /><attachment idref="CHEM-US-00268" attachment-type="mol" file="US08809264-20140819-C00268.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-20</entry><entry><chemistry id="CHEM-US-00269" num="00269"><img id="EMI-C00269" he="34.97mm" wi="34.71mm" file="US08809264-20140819-C00269.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00269" attachment-type="cdx" file="US08809264-20140819-C00269.CDX" /><attachment idref="CHEM-US-00269" attachment-type="mol" file="US08809264-20140819-C00269.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-21</entry><entry><chemistry id="CHEM-US-00270" num="00270"><img id="EMI-C00270" he="30.99mm" wi="38.27mm" file="US08809264-20140819-C00270.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00270" attachment-type="cdx" file="US08809264-20140819-C00270.CDX" /><attachment idref="CHEM-US-00270" attachment-type="mol" file="US08809264-20140819-C00270.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-22</entry><entry><chemistry id="CHEM-US-00271" num="00271"><img id="EMI-C00271" he="23.54mm" wi="30.31mm" file="US08809264-20140819-C00271.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00271" attachment-type="cdx" file="US08809264-20140819-C00271.CDX" /><attachment idref="CHEM-US-00271" attachment-type="mol" file="US08809264-20140819-C00271.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-23</entry><entry><chemistry id="CHEM-US-00272" num="00272"><img id="EMI-C00272" he="31.24mm" wi="34.46mm" file="US08809264-20140819-C00272.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00272" attachment-type="cdx" file="US08809264-20140819-C00272.CDX" /><attachment idref="CHEM-US-00272" attachment-type="mol" file="US08809264-20140819-C00272.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-24</entry><entry><chemistry id="CHEM-US-00273" num="00273"><img id="EMI-C00273" he="23.54mm" wi="39.37mm" file="US08809264-20140819-C00273.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00273" attachment-type="cdx" file="US08809264-20140819-C00273.CDX" /><attachment idref="CHEM-US-00273" attachment-type="mol" file="US08809264-20140819-C00273.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-25</entry><entry><chemistry id="CHEM-US-00274" num="00274"><img id="EMI-C00274" he="25.48mm" wi="39.37mm" file="US08809264-20140819-C00274.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00274" attachment-type="cdx" file="US08809264-20140819-C00274.CDX" /><attachment idref="CHEM-US-00274" attachment-type="mol" file="US08809264-20140819-C00274.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-26</entry><entry><chemistry id="CHEM-US-00275" num="00275"><img id="EMI-C00275" he="28.28mm" wi="39.37mm" file="US08809264-20140819-C00275.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00275" attachment-type="cdx" file="US08809264-20140819-C00275.CDX" /><attachment idref="CHEM-US-00275" attachment-type="mol" file="US08809264-20140819-C00275.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-27</entry><entry><chemistry id="CHEM-US-00276" num="00276"><img id="EMI-C00276" he="31.24mm" wi="44.28mm" file="US08809264-20140819-C00276.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00276" attachment-type="cdx" file="US08809264-20140819-C00276.CDX" /><attachment idref="CHEM-US-00276" attachment-type="mol" file="US08809264-20140819-C00276.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-28</entry><entry><chemistry id="CHEM-US-00277" num="00277"><img id="EMI-C00277" he="25.48mm" wi="39.37mm" file="US08809264-20140819-C00277.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00277" attachment-type="cdx" file="US08809264-20140819-C00277.CDX" /><attachment idref="CHEM-US-00277" attachment-type="mol" file="US08809264-20140819-C00277.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-29</entry><entry><chemistry id="CHEM-US-00278" num="00278"><img id="EMI-C00278" he="25.48mm" wi="39.29mm" file="US08809264-20140819-C00278.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00278" attachment-type="cdx" file="US08809264-20140819-C00278.CDX" /><attachment idref="CHEM-US-00278" attachment-type="mol" file="US08809264-20140819-C00278.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-30</entry><entry><chemistry id="CHEM-US-00279" num="00279"><img id="EMI-C00279" he="25.48mm" wi="44.20mm" file="US08809264-20140819-C00279.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00279" attachment-type="cdx" file="US08809264-20140819-C00279.CDX" /><attachment idref="CHEM-US-00279" attachment-type="mol" file="US08809264-20140819-C00279.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-31</entry><entry><chemistry id="CHEM-US-00280" num="00280"><img id="EMI-C00280" he="31.24mm" wi="34.46mm" file="US08809264-20140819-C00280.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00280" attachment-type="cdx" file="US08809264-20140819-C00280.CDX" /><attachment idref="CHEM-US-00280" attachment-type="mol" file="US08809264-20140819-C00280.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-32</entry><entry><chemistry id="CHEM-US-00281" num="00281"><img id="EMI-C00281" he="31.24mm" wi="35.31mm" file="US08809264-20140819-C00281.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00281" attachment-type="cdx" file="US08809264-20140819-C00281.CDX" /><attachment idref="CHEM-US-00281" attachment-type="mol" file="US08809264-20140819-C00281.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-33</entry><entry><chemistry id="CHEM-US-00282" num="00282"><img id="EMI-C00282" he="31.24mm" wi="35.39mm" file="US08809264-20140819-C00282.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00282" attachment-type="cdx" file="US08809264-20140819-C00282.CDX" /><attachment idref="CHEM-US-00282" attachment-type="mol" file="US08809264-20140819-C00282.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-34</entry><entry><chemistry id="CHEM-US-00283" num="00283"><img id="EMI-C00283" he="25.48mm" wi="49.11mm" file="US08809264-20140819-C00283.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00283" attachment-type="cdx" file="US08809264-20140819-C00283.CDX" /><attachment idref="CHEM-US-00283" attachment-type="mol" file="US08809264-20140819-C00283.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-35</entry><entry><chemistry id="CHEM-US-00284" num="00284"><img id="EMI-C00284" he="25.48mm" wi="35.31mm" file="US08809264-20140819-C00284.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00284" attachment-type="cdx" file="US08809264-20140819-C00284.CDX" /><attachment idref="CHEM-US-00284" attachment-type="mol" file="US08809264-20140819-C00284.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-36</entry><entry><chemistry id="CHEM-US-00285" num="00285"><img id="EMI-C00285" he="23.54mm" wi="30.31mm" file="US08809264-20140819-C00285.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00285" attachment-type="cdx" file="US08809264-20140819-C00285.CDX" /><attachment idref="CHEM-US-00285" attachment-type="mol" file="US08809264-20140819-C00285.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-37</entry><entry><chemistry id="CHEM-US-00286" num="00286"><img id="EMI-C00286" he="31.24mm" wi="44.28mm" file="US08809264-20140819-C00286.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00286" attachment-type="cdx" file="US08809264-20140819-C00286.CDX" /><attachment idref="CHEM-US-00286" attachment-type="mol" file="US08809264-20140819-C00286.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-38</entry><entry><chemistry id="CHEM-US-00287" num="00287"><img id="EMI-C00287" he="30.14mm" wi="43.18mm" file="US08809264-20140819-C00287.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00287" attachment-type="cdx" file="US08809264-20140819-C00287.CDX" /><attachment idref="CHEM-US-00287" attachment-type="mol" file="US08809264-20140819-C00287.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-39</entry><entry><chemistry id="CHEM-US-00288" num="00288"><img id="EMI-C00288" he="25.48mm" wi="49.11mm" file="US08809264-20140819-C00288.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00288" attachment-type="cdx" file="US08809264-20140819-C00288.CDX" /><attachment idref="CHEM-US-00288" attachment-type="mol" file="US08809264-20140819-C00288.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-40</entry><entry><chemistry id="CHEM-US-00289" num="00289"><img id="EMI-C00289" he="25.48mm" wi="38.27mm" file="US08809264-20140819-C00289.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00289" attachment-type="cdx" file="US08809264-20140819-C00289.CDX" /><attachment idref="CHEM-US-00289" attachment-type="mol" file="US08809264-20140819-C00289.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-41</entry><entry><chemistry id="CHEM-US-00290" num="00290"><img id="EMI-C00290" he="31.24mm" wi="44.28mm" file="US08809264-20140819-C00290.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00290" attachment-type="cdx" file="US08809264-20140819-C00290.CDX" /><attachment idref="CHEM-US-00290" attachment-type="mol" file="US08809264-20140819-C00290.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-42</entry><entry><chemistry id="CHEM-US-00291" num="00291"><img id="EMI-C00291" he="30.14mm" wi="43.18mm" file="US08809264-20140819-C00291.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00291" attachment-type="cdx" file="US08809264-20140819-C00291.CDX" /><attachment idref="CHEM-US-00291" attachment-type="mol" file="US08809264-20140819-C00291.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-43</entry><entry><chemistry id="CHEM-US-00292" num="00292"><img id="EMI-C00292" he="30.14mm" wi="43.18mm" file="US08809264-20140819-C00292.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00292" attachment-type="cdx" file="US08809264-20140819-C00292.CDX" /><attachment idref="CHEM-US-00292" attachment-type="mol" file="US08809264-20140819-C00292.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-44</entry><entry><chemistry id="CHEM-US-00293" num="00293"><img id="EMI-C00293" he="30.14mm" wi="49.70mm" file="US08809264-20140819-C00293.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00293" attachment-type="cdx" file="US08809264-20140819-C00293.CDX" /><attachment idref="CHEM-US-00293" attachment-type="mol" file="US08809264-20140819-C00293.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-45</entry><entry><chemistry id="CHEM-US-00294" num="00294"><img id="EMI-C00294" he="31.16mm" wi="43.18mm" file="US08809264-20140819-C00294.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00294" attachment-type="cdx" file="US08809264-20140819-C00294.CDX" /><attachment idref="CHEM-US-00294" attachment-type="mol" file="US08809264-20140819-C00294.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-46</entry><entry><chemistry id="CHEM-US-00295" num="00295"><img id="EMI-C00295" he="31.24mm" wi="44.28mm" file="US08809264-20140819-C00295.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00295" attachment-type="cdx" file="US08809264-20140819-C00295.CDX" /><attachment idref="CHEM-US-00295" attachment-type="mol" file="US08809264-20140819-C00295.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-47</entry><entry><chemistry id="CHEM-US-00296" num="00296"><img id="EMI-C00296" he="30.14mm" wi="43.18mm" file="US08809264-20140819-C00296.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00296" attachment-type="cdx" file="US08809264-20140819-C00296.CDX" /><attachment idref="CHEM-US-00296" attachment-type="mol" file="US08809264-20140819-C00296.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-48</entry><entry><chemistry id="CHEM-US-00297" num="00297"><img id="EMI-C00297" he="30.14mm" wi="43.18mm" file="US08809264-20140819-C00297.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00297" attachment-type="cdx" file="US08809264-20140819-C00297.CDX" /><attachment idref="CHEM-US-00297" attachment-type="mol" file="US08809264-20140819-C00297.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-49</entry><entry><chemistry id="CHEM-US-00298" num="00298"><img id="EMI-C00298" he="30.14mm" wi="43.18mm" file="US08809264-20140819-C00298.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00298" attachment-type="cdx" file="US08809264-20140819-C00298.CDX" /><attachment idref="CHEM-US-00298" attachment-type="mol" file="US08809264-20140819-C00298.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-50</entry><entry><chemistry id="CHEM-US-00299" num="00299"><img id="EMI-C00299" he="31.16mm" wi="43.18mm" file="US08809264-20140819-C00299.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00299" attachment-type="cdx" file="US08809264-20140819-C00299.CDX" /><attachment idref="CHEM-US-00299" attachment-type="mol" file="US08809264-20140819-C00299.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-51</entry><entry><chemistry id="CHEM-US-00300" num="00300"><img id="EMI-C00300" he="31.24mm" wi="44.28mm" file="US08809264-20140819-C00300.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00300" attachment-type="cdx" file="US08809264-20140819-C00300.CDX" /><attachment idref="CHEM-US-00300" attachment-type="mol" file="US08809264-20140819-C00300.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-52</entry><entry><chemistry id="CHEM-US-00301" num="00301"><img id="EMI-C00301" he="31.24mm" wi="45.13mm" file="US08809264-20140819-C00301.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00301" attachment-type="cdx" file="US08809264-20140819-C00301.CDX" /><attachment idref="CHEM-US-00301" attachment-type="mol" file="US08809264-20140819-C00301.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-53</entry><entry><chemistry id="CHEM-US-00302" num="00302"><img id="EMI-C00302" he="36.75mm" wi="49.95mm" file="US08809264-20140819-C00302.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00302" attachment-type="cdx" file="US08809264-20140819-C00302.CDX" /><attachment idref="CHEM-US-00302" attachment-type="mol" file="US08809264-20140819-C00302.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-54</entry><entry><chemistry id="CHEM-US-00303" num="00303"><img id="EMI-C00303" he="36.75mm" wi="54.02mm" file="US08809264-20140819-C00303.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00303" attachment-type="cdx" file="US08809264-20140819-C00303.CDX" /><attachment idref="CHEM-US-00303" attachment-type="mol" file="US08809264-20140819-C00303.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-55</entry><entry><chemistry id="CHEM-US-00304" num="00304"><img id="EMI-C00304" he="32.60mm" wi="46.48mm" file="US08809264-20140819-C00304.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00304" attachment-type="cdx" file="US08809264-20140819-C00304.CDX" /><attachment idref="CHEM-US-00304" attachment-type="mol" file="US08809264-20140819-C00304.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-56</entry><entry><chemistry id="CHEM-US-00305" num="00305"><img id="EMI-C00305" he="32.60mm" wi="46.48mm" file="US08809264-20140819-C00305.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00305" attachment-type="cdx" file="US08809264-20140819-C00305.CDX" /><attachment idref="CHEM-US-00305" attachment-type="mol" file="US08809264-20140819-C00305.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-57</entry><entry><chemistry id="CHEM-US-00306" num="00306"><img id="EMI-C00306" he="35.56mm" wi="52.75mm" file="US08809264-20140819-C00306.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00306" attachment-type="cdx" file="US08809264-20140819-C00306.CDX" /><attachment idref="CHEM-US-00306" attachment-type="mol" file="US08809264-20140819-C00306.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-58</entry><entry><chemistry id="CHEM-US-00307" num="00307"><img id="EMI-C00307" he="40.47mm" wi="34.46mm" file="US08809264-20140819-C00307.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00307" attachment-type="cdx" file="US08809264-20140819-C00307.CDX" /><attachment idref="CHEM-US-00307" attachment-type="mol" file="US08809264-20140819-C00307.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-59</entry><entry><chemistry id="CHEM-US-00308" num="00308"><img id="EMI-C00308" he="28.87mm" wi="39.29mm" file="US08809264-20140819-C00308.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00308" attachment-type="cdx" file="US08809264-20140819-C00308.CDX" /><attachment idref="CHEM-US-00308" attachment-type="mol" file="US08809264-20140819-C00308.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-60</entry><entry><chemistry id="CHEM-US-00309" num="00309"><img id="EMI-C00309" he="31.16mm" wi="39.37mm" file="US08809264-20140819-C00309.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00309" attachment-type="cdx" file="US08809264-20140819-C00309.CDX" /><attachment idref="CHEM-US-00309" attachment-type="mol" file="US08809264-20140819-C00309.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-61</entry><entry><chemistry id="CHEM-US-00310" num="00310"><img id="EMI-C00310" he="28.28mm" wi="45.04mm" file="US08809264-20140819-C00310.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00310" attachment-type="cdx" file="US08809264-20140819-C00310.CDX" /><attachment idref="CHEM-US-00310" attachment-type="mol" file="US08809264-20140819-C00310.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-62</entry><entry><chemistry id="CHEM-US-00311" num="00311"><img id="EMI-C00311" he="25.48mm" wi="45.04mm" file="US08809264-20140819-C00311.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00311" attachment-type="cdx" file="US08809264-20140819-C00311.CDX" /><attachment idref="CHEM-US-00311" attachment-type="mol" file="US08809264-20140819-C00311.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-63</entry><entry><chemistry id="CHEM-US-00312" num="00312"><img id="EMI-C00312" he="28.87mm" wi="39.29mm" file="US08809264-20140819-C00312.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00312" attachment-type="cdx" file="US08809264-20140819-C00312.CDX" /><attachment idref="CHEM-US-00312" attachment-type="mol" file="US08809264-20140819-C00312.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-64</entry><entry><chemistry id="CHEM-US-00313" num="00313"><img id="EMI-C00313" he="30.14mm" wi="43.18mm" file="US08809264-20140819-C00313.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00313" attachment-type="cdx" file="US08809264-20140819-C00313.CDX" /><attachment idref="CHEM-US-00313" attachment-type="mol" file="US08809264-20140819-C00313.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-65</entry><entry><chemistry id="CHEM-US-00314" num="00314"><img id="EMI-C00314" he="38.61mm" wi="30.31mm" file="US08809264-20140819-C00314.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00314" attachment-type="cdx" file="US08809264-20140819-C00314.CDX" /><attachment idref="CHEM-US-00314" attachment-type="mol" file="US08809264-20140819-C00314.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-66</entry><entry><chemistry id="CHEM-US-00315" num="00315"><img id="EMI-C00315" he="30.14mm" wi="43.77mm" file="US08809264-20140819-C00315.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00315" attachment-type="cdx" file="US08809264-20140819-C00315.CDX" /><attachment idref="CHEM-US-00315" attachment-type="mol" file="US08809264-20140819-C00315.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-67</entry><entry><chemistry id="CHEM-US-00316" num="00316"><img id="EMI-C00316" he="25.48mm" wi="43.10mm" file="US08809264-20140819-C00316.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00316" attachment-type="cdx" file="US08809264-20140819-C00316.CDX" /><attachment idref="CHEM-US-00316" attachment-type="mol" file="US08809264-20140819-C00316.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>Q-68</entry><entry><chemistry id="CHEM-US-00317" num="00317"><img id="EMI-C00317" he="25.48mm" wi="46.99mm" file="US08809264-20140819-C00317.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00317" attachment-type="cdx" file="US08809264-20140819-C00317.CDX" /><attachment idref="CHEM-US-00317" attachment-type="mol" file="US08809264-20140819-C00317.MOL" /></attachments></chemistry></entry></row><row><entry namest="1" nameend="3" align="center" rowsep="1" /></row></tbody></tgroup></table></tables>

<tables id="TABLE-US-00004" num="00004"><table frame="none" colsep="0" rowsep="0"><tgroup align="left" colsep="0" rowsep="0" cols="1"><colspec colname="1" colwidth="217pt" align="center" /><thead><row><entry namest="1" nameend="1" rowsep="1">TABLE 4</entry></row><row><entry namest="1" nameend="1" align="center" rowsep="1" /></row><row><entry>G-Matrix</entry></row><row><entry namest="1" nameend="1" align="center" rowsep="1" /></row></thead><tbody valign="top"><row><entry /></row></tbody></tgroup><tgroup align="left" colsep="0" rowsep="0" cols="3"><colspec colname="1" colwidth="28pt" align="left" /><colspec colname="2" colwidth="21pt" align="center" /><colspec colname="3" colwidth="168pt" align="center" /><tbody valign="top"><row><entry /><entry>G01</entry><entry>—OH</entry></row><row><entry></entry></row><row><entry /><entry>G02</entry><entry><chemistry id="CHEM-US-00318" num="00318"><img id="EMI-C00318" he="13.80mm" wi="23.45mm" file="US08809264-20140819-C00318.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00318" attachment-type="cdx" file="US08809264-20140819-C00318.CDX" /><attachment idref="CHEM-US-00318" attachment-type="mol" file="US08809264-20140819-C00318.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G03</entry><entry><chemistry id="CHEM-US-00319" num="00319"><img id="EMI-C00319" he="17.36mm" wi="27.52mm" file="US08809264-20140819-C00319.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00319" attachment-type="cdx" file="US08809264-20140819-C00319.CDX" /><attachment idref="CHEM-US-00319" attachment-type="mol" file="US08809264-20140819-C00319.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G04</entry><entry><chemistry id="CHEM-US-00320" num="00320"><img id="EMI-C00320" he="17.36mm" wi="28.28mm" file="US08809264-20140819-C00320.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00320" attachment-type="cdx" file="US08809264-20140819-C00320.CDX" /><attachment idref="CHEM-US-00320" attachment-type="mol" file="US08809264-20140819-C00320.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G05</entry><entry><chemistry id="CHEM-US-00321" num="00321"><img id="EMI-C00321" he="18.80mm" wi="35.81mm" file="US08809264-20140819-C00321.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00321" attachment-type="cdx" file="US08809264-20140819-C00321.CDX" /><attachment idref="CHEM-US-00321" attachment-type="mol" file="US08809264-20140819-C00321.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G06</entry><entry><chemistry id="CHEM-US-00322" num="00322"><img id="EMI-C00322" he="23.79mm" wi="42.16mm" file="US08809264-20140819-C00322.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00322" attachment-type="cdx" file="US08809264-20140819-C00322.CDX" /><attachment idref="CHEM-US-00322" attachment-type="mol" file="US08809264-20140819-C00322.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G07</entry><entry><chemistry id="CHEM-US-00323" num="00323"><img id="EMI-C00323" he="20.49mm" wi="35.14mm" file="US08809264-20140819-C00323.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00323" attachment-type="cdx" file="US08809264-20140819-C00323.CDX" /><attachment idref="CHEM-US-00323" attachment-type="mol" file="US08809264-20140819-C00323.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G08</entry><entry><chemistry id="CHEM-US-00324" num="00324"><img id="EMI-C00324" he="16.26mm" wi="42.76mm" file="US08809264-20140819-C00324.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00324" attachment-type="cdx" file="US08809264-20140819-C00324.CDX" /><attachment idref="CHEM-US-00324" attachment-type="mol" file="US08809264-20140819-C00324.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G09</entry><entry><chemistry id="CHEM-US-00325" num="00325"><img id="EMI-C00325" he="16.26mm" wi="26.42mm" file="US08809264-20140819-C00325.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00325" attachment-type="cdx" file="US08809264-20140819-C00325.CDX" /><attachment idref="CHEM-US-00325" attachment-type="mol" file="US08809264-20140819-C00325.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G10</entry><entry><chemistry id="CHEM-US-00326" num="00326"><img id="EMI-C00326" he="18.80mm" wi="35.81mm" file="US08809264-20140819-C00326.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00326" attachment-type="cdx" file="US08809264-20140819-C00326.CDX" /><attachment idref="CHEM-US-00326" attachment-type="mol" file="US08809264-20140819-C00326.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G11</entry><entry><chemistry id="CHEM-US-00327" num="00327"><img id="EMI-C00327" he="18.71mm" wi="37.59mm" file="US08809264-20140819-C00327.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00327" attachment-type="cdx" file="US08809264-20140819-C00327.CDX" /><attachment idref="CHEM-US-00327" attachment-type="mol" file="US08809264-20140819-C00327.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G12</entry><entry><chemistry id="CHEM-US-00328" num="00328"><img id="EMI-C00328" he="18.80mm" wi="37.59mm" file="US08809264-20140819-C00328.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00328" attachment-type="cdx" file="US08809264-20140819-C00328.CDX" /><attachment idref="CHEM-US-00328" attachment-type="mol" file="US08809264-20140819-C00328.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G13</entry><entry><chemistry id="CHEM-US-00329" num="00329"><img id="EMI-C00329" he="18.80mm" wi="35.81mm" file="US08809264-20140819-C00329.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00329" attachment-type="cdx" file="US08809264-20140819-C00329.CDX" /><attachment idref="CHEM-US-00329" attachment-type="mol" file="US08809264-20140819-C00329.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G14</entry><entry><chemistry id="CHEM-US-00330" num="00330"><img id="EMI-C00330" he="18.97mm" wi="27.52mm" file="US08809264-20140819-C00330.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00330" attachment-type="cdx" file="US08809264-20140819-C00330.CDX" /><attachment idref="CHEM-US-00330" attachment-type="mol" file="US08809264-20140819-C00330.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G15</entry><entry><chemistry id="CHEM-US-00331" num="00331"><img id="EMI-C00331" he="16.26mm" wi="42.76mm" file="US08809264-20140819-C00331.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00331" attachment-type="cdx" file="US08809264-20140819-C00331.CDX" /><attachment idref="CHEM-US-00331" attachment-type="mol" file="US08809264-20140819-C00331.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G16</entry><entry><chemistry id="CHEM-US-00332" num="00332"><img id="EMI-C00332" he="11.60mm" wi="20.74mm" file="US08809264-20140819-C00332.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00332" attachment-type="cdx" file="US08809264-20140819-C00332.CDX" /><attachment idref="CHEM-US-00332" attachment-type="mol" file="US08809264-20140819-C00332.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G17</entry><entry><chemistry id="CHEM-US-00333" num="00333"><img id="EMI-C00333" he="18.20mm" wi="33.87mm" file="US08809264-20140819-C00333.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00333" attachment-type="cdx" file="US08809264-20140819-C00333.CDX" /><attachment idref="CHEM-US-00333" attachment-type="mol" file="US08809264-20140819-C00333.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G18</entry><entry><chemistry id="CHEM-US-00334" num="00334"><img id="EMI-C00334" he="18.12mm" wi="27.52mm" file="US08809264-20140819-C00334.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00334" attachment-type="cdx" file="US08809264-20140819-C00334.CDX" /><attachment idref="CHEM-US-00334" attachment-type="mol" file="US08809264-20140819-C00334.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G19</entry><entry><chemistry id="CHEM-US-00335" num="00335"><img id="EMI-C00335" he="11.60mm" wi="21.34mm" file="US08809264-20140819-C00335.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00335" attachment-type="cdx" file="US08809264-20140819-C00335.CDX" /><attachment idref="CHEM-US-00335" attachment-type="mol" file="US08809264-20140819-C00335.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G20</entry><entry><chemistry id="CHEM-US-00336" num="00336"><img id="EMI-C00336" he="21.08mm" wi="26.42mm" file="US08809264-20140819-C00336.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00336" attachment-type="cdx" file="US08809264-20140819-C00336.CDX" /><attachment idref="CHEM-US-00336" attachment-type="mol" file="US08809264-20140819-C00336.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G21</entry><entry><chemistry id="CHEM-US-00337" num="00337"><img id="EMI-C00337" he="15.92mm" wi="26.08mm" file="US08809264-20140819-C00337.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00337" attachment-type="cdx" file="US08809264-20140819-C00337.CDX" /><attachment idref="CHEM-US-00337" attachment-type="mol" file="US08809264-20140819-C00337.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G22</entry><entry><chemistry id="CHEM-US-00338" num="00338"><img id="EMI-C00338" he="18.20mm" wi="33.87mm" file="US08809264-20140819-C00338.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00338" attachment-type="cdx" file="US08809264-20140819-C00338.CDX" /><attachment idref="CHEM-US-00338" attachment-type="mol" file="US08809264-20140819-C00338.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G23</entry><entry><chemistry id="CHEM-US-00339" num="00339"><img id="EMI-C00339" he="17.36mm" wi="33.02mm" file="US08809264-20140819-C00339.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00339" attachment-type="cdx" file="US08809264-20140819-C00339.CDX" /><attachment idref="CHEM-US-00339" attachment-type="mol" file="US08809264-20140819-C00339.MOL" /></attachments></chemistry></entry></row><row><entry></entry></row><row><entry /><entry>G24</entry><entry><chemistry id="CHEM-US-00340" num="00340"><img id="EMI-C00340" he="13.21mm" wi="31.33mm" file="US08809264-20140819-C00340.TIF" alt="embedded image" img-content="table" img-format="tif" 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id="CHEM-US-00344" num="00344"><img id="EMI-C00344" he="13.80mm" wi="33.53mm" file="US08809264-20140819-C00344.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00344" attachment-type="cdx" file="US08809264-20140819-C00344.CDX" /><attachment idref="CHEM-US-00344" attachment-type="mol" file="US08809264-20140819-C00344.MOL" /></attachments></chemistry></entry></row><row><entry namest="1" nameend="3" align="center" rowsep="1" /></row></tbody></tgroup></table></tables>

In an additional aspect, the invention provides compounds of Formula V A compound of Formula V:

<chemistry id="CHEM-US-00345" num="00345"><img id="EMI-C00345" he="61.81mm" wi="69.85mm" file="US08809264-20140819-C00345.TIF" alt="embedded image" img-content="chem" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00345" attachment-type="cdx" file="US08809264-20140819-C00345.CDX" /><attachment idref="CHEM-US-00345" attachment-type="mol" file="US08809264-20140819-C00345.MOL" /></attachments></chemistry> in which

A is selected from H, —(C═O)—O—R1, —(C═O)—R2, —C(═O)—NH—R2, or —S(O)2—R1, —S(O)2NHR2;

each R1 is independently selected from the group consisting of: <ul><li id="ul0013-0001" num="0000"><ul><li id="ul0014-0001" num="0090">(i) aryl; substituted aryl; heteroaryl; substituted heteroaryl;</li><li id="ul0014-0002" num="0091">(ii) heterocycloalkyl or substituted heterocycloalkyl;</li><li id="ul0014-0003" num="0092">(iii) —C1-C8 alkyl, —C2-C8 alkenyl, or —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N; substituted —C1-C8 alkyl, substituted —C2-C8 alkenyl, or substituted —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N; —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkyl; —C3-C12 cycloalkenyl, or substituted —C3-C12 cycloalkenyl;</li></ul></li></ul>

each R2 is independently selected from the group consisting of: <ul><li id="ul0015-0001" num="0000"><ul><li id="ul0016-0001" num="0094">(i) hydrogen;</li><li id="ul0016-0002" num="0095">(ii) aryl; substituted aryl; heteroaryl; substituted heteroaryl;</li><li id="ul0016-0003" num="0096">(iii) heterocycloalkyl or substituted heterocycloalkyl;</li><li id="ul0016-0004" num="0097">(iv) —C1-C8 alkyl, —C2-C8 alkenyl, or —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N; substituted —C1-C8 alkyl, substituted —C2-C8 alkenyl, or substituted —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N; —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkyl; —C3-C12 cycloalkenyl, or substituted —C3-C12 cycloalkenyl;</li></ul></li></ul>

G is selected from —NHS(O)2—R3 and —NH(SO2)NR4R5;

each R3 is independently selected from: <ul><li id="ul0017-0001" num="0000"><ul><li id="ul0018-0001" num="0100">(i) aryl; substituted aryl; heteroaryl; substituted heteroaryl</li><li id="ul0018-0002" num="0101">(ii) heterocycloalkyl or substituted heterocycloalkyl;</li><li id="ul0018-0003" num="0102">(iii) —C1-C8 alkyl, —C2-C8 alkenyl, or —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N, substituted —C1-C8 alkyl, substituted —C2-C8 alkenyl, or substituted —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N; —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkyl; —C3-C12 cycloalkenyl, or substituted —C3-C12 cycloalkenyl;</li></ul></li></ul>

each R4 and R5 is independently selected from: <ul><li id="ul0019-0001" num="0000"><ul><li id="ul0020-0001" num="0104">(i) hydrogen;</li><li id="ul0020-0002" num="0105">(ii) aryl; substituted aryl; heteroaryl; substituted heteroaryl;</li><li id="ul0020-0003" num="0106">(iii) heterocycloalkyl or substituted heterocycloalkyl;</li><li id="ul0020-0004" num="0107">(iv) —C1-C8 alkyl, —C2-C8 alkenyl, or —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N; substituted —C1-C8 alkyl, substituted —C2-C8 alkenyl, or substituted —C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N; —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkyl; —C3-C12 cycloalkenyl, or substituted —C3-C12 cycloalkenyl;</li></ul></li></ul>

L is selected from —CH2—, —O—, —S—, or —S(O)2—;

X and Y taken together with the carbon atoms to which they are attached to form a cyclic moiety selected from aryl, substituted aryl, heteroaryl, or substituted heteroaryl;

W is absent, or selected from —O—, —S—, —NH—, —N(Me)-, —C(O)NH—, or —C(O)N(Me)-;

Z is selected from the groups consisting of: <ul><li id="ul0021-0001" num="0000"><ul><li id="ul0022-0001" num="0112">(i) hydrogen;</li><li id="ul0022-0002" num="0113">(ii) —CN;</li><li id="ul0022-0003" num="0114">(iii) —N3;</li><li id="ul0022-0004" num="0115">(iv) halogen;</li><li id="ul0022-0005" num="0116">(v) —NH—N═CH(R2), where R2 is as defined above;</li><li id="ul0022-0006" num="0117">(vi) aryl, substituted aryl;</li><li id="ul0022-0007" num="0118">(vii) heteroaryl, substituted heteroaryl;</li><li id="ul0022-0008" num="0119">(viii) —C3-C12 cycloalkyl, substituted —C3-C12 cycloalkyl, heterocycloalkyl, substituted heterocycloalkyl;</li><li id="ul0022-0009" num="0120">(ix) —C1-C6 alkyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;</li><li id="ul0022-0010" num="0121">(x) —C2-C6 alkenyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;</li><li id="ul0022-0011" num="0122">(xi) —C2-C6 alkynyl containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;</li></ul></li></ul>

j=0, 1, 2, 3, or 4;

k=1, 2, or 3;

m=0, 1, or 2; and

<img id="CUSTOM-CHARACTER-00002" he="3.13mm" wi="6.35mm" file="US08809264-20140819-P00001.TIF" alt="custom character" img-content="character" img-format="tif" orientation="portrait" inline="no" /> denotes a carbon-carbon single or double bond.

In one example, L is —CH2—, j is 2, and k is 1. A is selected from the group consisting of —C(O)—R2, —C(O)—O—R2, —S(O)2NHR2 and —C(O)—NH—R2, where R2 is selected from aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic, —C1-C8 alkyl, —C2-C8 alkenyl, —C2-C8 alkynyl, substituted —C1-C8 alkyl, substituted —C2-C8 alkenyl, substituted —C2-C8 alkynyl, —C3-C12 cycloalkyl, —C3-C12 cycloalkenyl, substituted —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkenyl. G can be —NH—SO2—NH—R3 or —NHSO2—R3, where R3 is selected from —C1-C8 alkyl, —C2-C8 alkenyl, —C2-C8 alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic, —C3-C12 cycloalkyl, —C3-C12 cycloalkenyl, substituted —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkenyl.

In still another example, L is —CH2—, j is 2, and k is 1. A is —C(O)—O—R2, —S(O)2NHR2 or —C(O)—NH—R2, where R2 is —C1-C8 alkyl, —C2-C8 alkenyl, —C2-C8 alkynyl, substituted —C1-C8 alkyl, substituted —C2-C8 alkenyl, substituted —C2-C8 alkynyl, —C3-C12 cycloalkyl, —C3-C12 cycloalkenyl, substituted —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkenyl. G is —NHSO2—R3, where R3 is selected from —C1-C8 alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic, —C3-C12 cycloalkyl, —C3-C12 cycloalkenyl, substituted —C3-C12 cycloalkyl, or substituted —C3-C12 cycloalkenyl.

In still yet another example, L is —CH2—, j is 2, and k is 1. W is absent. Z is heteroaryl, substitute heteroaryl, aryl, or substituted aryl. A is —C(O)—O—R1, where R1 is —C1-C8 alkyl, —C3-C12 cycloalkyl, substituted —C3-C12 cycloalkyl, heteroaryl, or substituted heteroaryl. G is —NHSO2—R3, where R3 is selected from —C3-C12 cycloalkyl or substituted —C3-C12 cycloalkyl.

In still another example, L is —CH2—, j is 2, and k is 1. W is absent. Z is heteroaryl, substitute heteroaryl. A is —C(O)—O—R1, where R1 is —C1-C8 alkyl, —C3-C12 cycloalkyl, substituted —C3-C12 cycloalkyl, heteroaryl, or substituted heteroaryl. G is —NHSO2—R3, where R3 is selected from —C3-C12 cycloalkyl or substituted —C3-C12 cycloalkyl.

The present invention also features pharmaceutical compositions comprising a compound of the invention (e.g., a compound of Formula I, II, II′, II″, III, IV, or V, as described hereinabove), or a pharmaceutically acceptable salt, ester or prodrug thereof.

According to an alternate embodiment, the pharmaceutical compositions of the present invention may further contain other anti-HCV agents, or may be administered (concurrently or sequentially) with other anti-HCV agents, e.g., as part of a combination therapy. Examples of anti-HCV agents include, but are not limited to, interferon (e.g., α-interferon, β-interferon, consensus interferon, pegylated interferon, or albumin or other conjugated interferon), ribavirin, and amantadine. For further details see S. Tan, A. Pause, Y. Shi, N. Sonenberg, Hepatitis C Therapeutics: Current Status and Emerging Strategies, Nature Rev. Drug Discov., 1, 867-881 (2002); WO 00/59929 (2000); WO 99/07733 (1999); WO 00/09543 (2000); WO 99/50230 (1999); U.S. Pat. No. 5,861,297 (1999); and US2002/0037998 (2002) which are herein incorporated by reference in their entirety.

According to an additional embodiment, the pharmaceutical compositions of the present invention may further contain other HCV protease inhibitors.

According to yet another embodiment, the pharmaceutical compositions of the present invention may further comprise inhibitor(s) of other targets in the HCV life cycle, including, but not limited to, helicase, polymerase, metalloprotease, and internal ribosome entry site (IRES).

According to a further embodiment, the present invention includes methods of treating hepatitis C infections in a subject in need of such treatment by administering to said subject an anti-HCV virally effective amount or an inhibitory amount of the pharmaceutical compositions of the present invention.

An additional embodiment of the present invention includes methods of treating biological samples by contacting the biological samples with the compounds of the present invention, e.g., to reduce the potential for infection by HCV which may be present in the sample.

Yet a further aspect of the present invention is a process of making any of the compounds delineated herein employing any of the synthetic means delineated herein.

DEFINITIONS

Listed below are definitions of various terms used to describe this invention. These definitions apply to the terms as they are used throughout this specification and claims, unless otherwise limited in specific instances, either individually or as part of a larger group.

The term “C1-C6 alkyl,” or “C1-C8 alkyl,” as used herein, refer to saturated, straight- or branched-chain hydrocarbon radicals containing between one and six, or one and eight carbon atoms, respectively. Examples of C1-C6 alkyl radicals include, but are not limited to, methyl, ethyl, propyl, isopropyl, n-butyl, tert-butyl, neopentyl, n-hexyl radicals; and examples of C1-C8 alkyl radicals include, but are not limited to, methyl, ethyl, propyl, isopropyl, n-butyl, tert-butyl, neopentyl, n-hexyl, heptyl, octyl radicals.

The term “C2-C6 alkenyl,” or “C2-C8 alkenyl,” as used herein, denote a monovalent group derived from a hydrocarbon moiety by the removal of a single hydrogen atom where the hydrocarbon moiety contains from two to six, or two to eight, carbon atoms, respectively, and has at least one carbon-carbon double bond. Alkenyl groups include, but are not limited to, for example, ethenyl, propenyl, butenyl, 1-methyl-2-buten-1-yl, heptenyl, octenyl and the like.

The term “C2-C6 alkynyl,” or “C2-C8 alkynyl,” as used herein, denote a monovalent group derived from a hydrocarbon moiety by the removal of a single hydrogen atom where the hydrocarbon moiety contains from two to six, or two to eight, carbon atoms, receptively, and has at least one carbon-carbon triple bond. Representative alkynyl groups include, but are not limited to, for example, ethynyl, 1-propynyl, 1-butynyl, heptynyl, octynyl and the like.

The term “C3-C8-cycloalkyl”, or “C3-C12-cycloalkyl,” as used herein, denotes a monovalent group derived from a monocyclic or polycyclic saturated carbocyclic ring compound by the removal of a single hydrogen atom wherein the carbocyclic ring has from 3 to 8 ring atoms, or from 3 to 12 ring atoms, respectively. Examples of C3-C8-cycloalkyl include, but not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopentyl and cyclooctyl; and examples of C3-C12-cycloalkyl include, but not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, bicyclo[2.2.1]heptyl, and bicyclo[2.2.2]octyl.

The term “C3-C8-cycloalkenyl”, or “C3-C12-cycloalkenyl” as used herein, denote a monovalent group derived from a monocyclic or polycyclic carbocyclic ring compound by the removal of a single hydrogen atom wherein the carbocyclic ring has having at least one carbon-carbon double bond and contains from 3 to 8 ring atoms, or from 3 to 12 ring atoms, respectively. Examples of C3-C8-cycloalkenyl include, but not limited to, cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl, and the like; and examples of C3-C12-cycloalkenyl include, but not limited to, cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl, and the like.

The term “aryl,” as used herein, refers to a mono- or bicyclic carbocyclic ring system having one or two aromatic rings including, but not limited to, phenyl, naphthyl, tetrahydronaphthyl, indanyl, idenyl and the like.

The term “arylalkyl,” as used herein, refers to a C1-C3 alkyl or C1-C6 alkyl residue attached to an aryl ring. Examples include, but are not limited to, benzyl, phenethyl and the like.

The term “heteroaryl,” as used herein, refers to a mono-, bi-, or tri-cyclic aromatic radical or ring having from five to ten ring atoms of which one ring atom is selected from S, O and N; zero, one or two ring atoms are additional heteroatoms independently selected from S, O and N; and the remaining ring atoms are carbon. Heteroaryl includes, but is not limited to, pyridinyl, pyrazinyl, pyrimidinyl, pyrrolyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl, isooxazolyl, thiadiazolyl, oxadiazolyl, thiophenyl, furanyl, quinolinyl, isoquinolinyl, benzimidazolyl, benzooxazolyl, quinoxalinyl, and the like.

The term “heteroarylalkyl,” as used herein, refers to a C1-C3 alkyl or C1-C6 alkyl residue residue attached to a heteroaryl ring. Examples include, but are not limited to, pyridinylmethyl, pyrimidinylethyl and the like.

The term “heterocycloalkyl,” as used herein, refers to a non-aromatic 3-, 4-, 5-, 6- or 7-membered ring or a bi- or tri-cyclic group fused system, where (i) each ring contains between one and three heteroatoms independently selected from oxygen, sulfur and nitrogen, (ii) each 5-membered ring has 0 to 1 double bonds and each 6-membered ring has 0 to 2 double bonds, (iii) the nitrogen and sulfur heteroatoms may optionally be oxidized, (iv) the nitrogen heteroatom may optionally be quaternized, and (iv) any of the above rings may be fused to a benzene ring. Representative heterocycloalkyl groups include, but are not limited to, [1,3]dioxolane, pyrrolidinyl, pyrazolinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, piperidinyl, piperazinyl, oxazolidinyl, isoxazolidinyl, morpholinyl, thiazolidinyl, isothiazolidinyl, and tetrahydrofuryl.

The term “substituted” as used herein, refers to independent replacement of one, two, or three or more of the hydrogen atoms thereon with substituents including, but not limited to, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, —COOH, —C(O)O—C1-C6 alkyl, —C(O)O—C2-C6 alkenyl, —C(O)O—C2-C6 alkynyl, —C(O)O-aryl, —C(O)O-substituted aryl, —C(O)O-heteroarylaryl, —C(O)O-substituted heteroaryl, —C(O)O—C3-C12-cycloalkyl, —C(O)O-heterocycloalkyl, —C(O)H, —F, —Cl, —Br, —I, —OH, protected hydroxy, —NO2, —CN, —NH2, protected amino, oxo, thioxo, —NH—C1-C12-alkyl, —NH—C2-C12-alkenyl, —NH—C2-C12-alkenyl, —NH—C3-C12-cycloalkyl, —NH-aryl, —NH-heteroaryl, —NH-heterocycloalkyl, -dialkylamino, -diarylamino, -diheteroarylamino, —O—C1-C12-alkyl, —O—C2-C12-alkenyl, —O—C2-C12-alkenyl, —O—C3-C12-cycloalkyl, —O-aryl, —O-heteroaryl, —O-heterocycloalkyl, —C(O)—C1-C12-alkyl, —C(O)—C2-C12-alkenyl, —C(O)—C2-C12-alkenyl, —C(O)—C3-C12-cycloalkyl, —C(O)-aryl, —C(O)-heteroaryl, —C(O)-heterocycloalkyl, —CONH2, —CONH—C1-C12-alkyl, —CONH—C2-C12-alkenyl, —CONH—C2-C12-alkenyl, —CONH—C3-C12-cycloalkyl, —CONH-aryl, —CONH-heteroaryl, —CONH-heterocycloalkyl, —OCO2—C1-C12-alkyl, —OCO2—C2-C12-alkenyl, —OCO2—C2-C12-alkenyl, —OCO2—C3-C12-cycloalkyl, —OCO2-aryl, —OCO2-heteroaryl, —OCO2-heterocycloalkyl, —OCONH2, —OCONH—C1-C12-alkyl, —OCONH—C2-C12-alkenyl, —OCONH—C2-C12-alkenyl, —OCONH—C3-C12-cycloalkyl, —OCONH-aryl, —OCONH-heteroaryl, —OCONH-heterocycloalkyl, —NHC(O)H, —NHC(O)—C1-C12-alkyl, —NHC(O)—C2-C12-alkenyl, —NHC(O)—C2-C12-alkenyl, —NHC(O)—C3-C12-cycloalkyl, —NHC(O)-aryl, —NHC(O)-heteroaryl, —NHC(O)-heterocycloalkyl, —NHCO2—C1-C12-alkyl, —NHCO2—C2-C12-alkenyl, —NHCO2—C2-C12-alkenyl, —NHCO2—C3-C12-cycloalkyl, —NHCO2-aryl, —NHCO2-heteroaryl, —NHCO2-heterocycloalkyl, —NHC(O)NH2, —NHC(O)NH—C1-C12-alkyl, —NHC(O)NH—C2-C12-alkenyl, —NHC(O)NH—C2-C12-alkenyl, —NHC(O)NH—C3-C12-cycloalkyl, —NHC(O)NH-aryl, —NHC(O)NH-heteroaryl, —NHC(O)NH-heterocycloalkyl, NHC(S)NH2, —NHC(S)NH—C1-C12-alkyl, —NHC(S)NH—C2-C12-alkenyl, —NHC(S)NH—C2-C12-alkenyl, —NHC(S)NH—C3-C12-cycloalkyl, —NHC(S)NH-aryl, —NHC(S)NH-heteroaryl, —NHC(S)NH-heterocycloalkyl, —NHC(NH)NH2, —NHC(NH)NH—C1-C12-alkyl, —NHC(NH)NH—C2-C12-alkenyl, —NHC(NH)NH—C2-C12-alkenyl, —NHC(NH)NH—C3-C12-cycloalkyl, —NHC(NH)NH-aryl, —NHC(NH)NH-heteroaryl, —NHC(NH)NH-heterocycloalkyl, —NHC(NH)—C1-C12-alkyl, —NHC(NH)—C2-C12-alkenyl, —NHC(NH)—C2-C12-alkenyl, —NHC(NH)—C3-C12-cycloalkyl, —NHC(NH)-aryl, —NHC(NH)-heteroaryl, —NHC(NH)-heterocycloalkyl, —C(NH)NH—C1-C12-alkyl, —C(NH)NH—C2-C12-alkenyl, —C(NH)NH—C2-C12-alkenyl, —C(NH)NH—C3-C12-cycloalkyl, —C(NH)NH-aryl, —C(NH)NH-heteroaryl, —C(NH)NH-heterocycloalkyl, —S(O)—C1-C12-alkyl, —S(O)—C2-C12-alkenyl, —S(O)—C2-C12-alkenyl, —S(O)—C3-C12-cycloalkyl, —S(O)-aryl, —S(O)-heteroaryl, S(O)-heterocycloalkyl-SO2NH2, —SO2NH—C1-C12-alkyl, —SO2NH—C2-C12-alkenyl, —SO2NH—C2-C12-alkenyl, —SO2NH—C3-C12-cycloalkyl, —SO2NH-aryl, —SO2NH-heteroaryl, —SO2NH-heterocycloalkyl, —NHSO2—C1-C12-alkyl, —NHSO2—C2-C12-alkenyl, —NHSO2—C2-C12-alkenyl, —NHSO2—C3-C12-cycloalkyl, —NHSO2-aryl, —NHSO2-heteroaryl, —NHSO2-heterocycloalkyl, —CH2NH2, —CH2SO2CH3, -aryl, -arylalkyl, -heteroaryl, -heteroarylalkyl, -heterocycloalkyl, —C3-C12-cycloalkyl, polyalkoxyalkyl, polyalkoxy, -methoxymethoxy, -methoxyethoxy, —SH, —S—C1-C12-alkyl, —S—C2-C12-alkenyl, —S—C2-C12-alkenyl, —S—C3-C12-cycloalkyl, —S-aryl, —S-heteroaryl, —S-heterocycloalkyl, methylthiomethyl, —Si(alkyl)3, or —Si(aryl)3. It is understood that the aryls, heteroaryls, alkyls, and the like can be further substituted. In some cases, each substituent in a substituted moiety is additionally optionally substituted with one or more groups, each group being independently selected from —F, —Cl, —Br, —I, —OH, —NO2, —CN, or —NH2.

In accordance with the invention, any of the aryls, substituted aryls, heteroaryls and substituted heteroaryls described herein, can be any aromatic group. Aromatic groups can be substituted or unsubstituted.

It is understood that any alkyl, alkenyl, alkynyl, cycloalkyl and cycloalkenyl moiety described herein can also be replaced by an aliphatic group, an alicyclic group or a heterocyclic group. An “aliphatic group” is non-aromatic moiety that may contain any combination of carbon atoms, hydrogen atoms, halogen atoms, oxygen, nitrogen or other atoms, and optionally contain one or more units of unsaturation, e.g., double and/or triple bonds. An aliphatic group may be straight chained, branched or cyclic and preferably contains between about 1 and about 24 carbon atoms, more typically between about 1 and about 12 carbon atoms. In addition to aliphatic hydrocarbon groups, aliphatic groups include, for example, polyalkoxyalkyls, such as polyalkylene glycols, polyamines, and polyimines, for example. Such aliphatic groups may be further substituted. It is understood that aliphatic groups may be used in place of the alkyl, alkenyl, alkynyl, alkylene, alkenylene, and alkynylene groups described herein.

The term “alicyclic,” as used herein, denotes a monovalent group derived from a monocyclic or polycyclic saturated carbocyclic ring compound by the removal of a single hydrogen atom. Examples include, but not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, bicyclo[2.2.1]heptyl, and bicyclo[2.2.2]octyl. Such alicyclic groups may be further substituted.

The terms “halo” and “halogen,” as used herein, refer to an atom selected from fluorine, chlorine, bromine and iodine.

The compounds described herein contain one or more asymmetric centers and thus give rise to enantiomers, diastereomers, and other stereoisomeric forms that may be defined, in terms of absolute stereochemistry, as (R)- or (S)-, or as (D)- or (L)- for amino acids. The present invention is meant to include all such possible isomers, as well as their racemic and optically pure forms. Optical isomers may be prepared from their respective optically active precursors by the procedures described above, or by resolving the racemic mixtures. The resolution can be carried out in the presence of a resolving agent, by chromatography or by repeated crystallization or by some combination of these techniques which are known to those skilled in the art. Further details regarding resolutions can be found in Jacques, et al., Enantiomers, Racemates, and Resolutions (John Wiley & Sons, 1981). When the compounds described herein contain olefinic double bonds or other centers of geometric asymmetry, and unless specified otherwise, it is intended that the compounds include both E and Z geometric isomers. Likewise, all tautomeric forms are also intended to be included. The configuration of any carbon-carbon double bond appearing herein is selected for convenience only and is not intended to designate a particular configuration unless the text so states; thus a carbon-carbon double bond depicted arbitrarily herein as trans may be cis, trans, or a mixture of the two in any proportion.

The term “subject” as used herein refers to a mammal. A subject therefore refers to, for example, dogs, cats, horses, cows, pigs, guinea pigs, and the like. Preferably the subject is a human. When the subject is a human, the subject may be referred to herein as a patient.

As used herein, the term “pharmaceutically acceptable salt” refers to those salts of the compounds formed by the process of the present invention which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio. Pharmaceutically acceptable salts are well known in the art. For example, S. M. Berge, et al. describes pharmaceutically acceptable salts in detail in J. Pharmaceutical Sciences, 66: 1-19 (1977). The salts can be prepared in situ during the final isolation and purification of the compounds of the invention, or separately by reacting the free base function with a suitable organic acid. Examples of pharmaceutically acceptable include, but are not limited to, nontoxic acid addition salts are salts of an amino group formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid or with organic acids such as acetic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange. Other pharmaceutically acceptable salts include, but are not limited to, adipate, alginate, ascorbate, aspartate, benzenesulfonate, benzoate, bisulfate, borate, butyrate, camphorate, camphorsulfonate, citrate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptonate, glycerophosphate, gluconate, hemisulfate, heptanoate, hexanoate, hydroiodide, 2-hydroxy-ethanesulfonate, lactobionate, lactate, laurate, lauryl sulfate, malate, maleate, malonate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, oleate, oxalate, palmitate, pamoate, pectinate, persulfate, 3-phenylpropionate, phosphate, picrate, pivalate, propionate, stearate, succinate, sulfate, tartrate, thiocyanate, p-toluenesulfonate, undecanoate, valerate salts, and the like. Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like. Further pharmaceutically acceptable salts include, when appropriate, nontoxic ammonium, quaternary ammonium, and amine cations formed using counterions such as halide, hydroxide, carboxylate, sulfate, phosphate, nitrate, alkyl having from 1 to 6 carbon atoms, sulfonate and aryl sulfonate.

As used herein, the term “pharmaceutically acceptable ester” refers to esters of the compounds formed by the process of the present invention which hydrolyze in vivo and include those that break down readily in the human body to leave the parent compound or a salt thereof. Suitable ester groups include, for example, those derived from pharmaceutically acceptable aliphatic carboxylic acids, particularly alkanoic, alkenoic, cycloalkanoic and alkanedioic acids, in which each alkyl or alkenyl moiety advantageously has not more than 6 carbon atoms. Examples of particular esters include, but are not limited to, formates, acetates, propionates, butyrates, acrylates and ethylsuccinates.

The term “pharmaceutically acceptable prodrugs” as used herein refers to those prodrugs of the compounds formed by the process of the present invention which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals with undue toxicity, irritation, allergic response, and the like, commensurate with a reasonable benefit/risk ratio, and effective for their intended use, as well as the zwitterionic forms, where possible, of the compounds of the present invention. “Prodrug”, as used herein means a compound which is convertible in vivo by metabolic means (e.g. by hydrolysis) to afford any compound delineated by the formulae of the instant invention. Various forms of prodrugs are known in the art, for example, as discussed in Bundgaard, (ed.), Design of Prodrugs, Elsevier (1985); Widder, et al. (ed.), Methods in Enzymology, vol. 4, Academic Press (1985); Krogsgaard-Larsen, et al., (ed). “Design and Application of Prodrugs, Textbook of Drug Design and Development, Chapter 5, 113-191 (1991); Bundgaard, et al., Journal of Drug Deliver Reviews, 8:1-38 (1992); Bundgaard, J. of Pharmaceutical Sciences, 77:285 et seq. (1988); Higuchi and Stella (eds.) Prodrugs as Novel Drug Delivery Systems, American Chemical Society (1975); and Bernard Testa & Joachim Mayer, “Hydrolysis In Drug And Prodrug Metabolism: Chemistry, Biochemistry And Enzymology,” John Wiley and Sons, Ltd. (2002).

Combinations of substituents and variables envisioned by this invention are only those that result in the formation of stable compounds. The term “stable”, as used herein, refers to compounds which possess stability sufficient to allow manufacture and which maintains the integrity of the compound for a sufficient period of time to be useful for the purposes detailed herein (e.g., therapeutic or prophylactic administration to a subject).

The synthesized compounds can be separated from a reaction mixture and further purified by a method such as column chromatography, high pressure liquid chromatography, or recrystallization. As can be appreciated by the skilled artisan, further methods of synthesizing the compounds of the formulae herein will be evident to those of ordinary skill in the art in the view of the present invention. Additionally, the various synthetic steps may be performed in an alternate sequence or order to give the desired compounds. In addition, the solvents, temperatures, reaction durations, etc. delineated herein are for purposes of illustration only and one of ordinary skill in the art will recognize that variation of the reaction conditions can produce the desired bridged macrocyclic products of the present invention. Synthetic chemistry transformations and protecting group methodologies (protection and deprotection) useful in synthesizing the compounds described herein are known in the art and include, for example, those such as described in R. Larock, Comprehensive Organic Transformations, VCH Publishers (1989); T. W. Greene and P. G. M. Wuts, Protective Groups in Organic Synthesis, 2d. Ed., John Wiley and Sons (1991); L. Fieser and M. Fieser, Fieser and Fieser's Reagents for Organic Synthesis, John Wiley and Sons (1994); and L. Paquette, ed., Encyclopedia of Reagents for Organic Synthesis, John Wiley and Sons (1995).

The compounds of this invention may be modified by appending various functionalities via any synthetic means delineated herein to enhance selective biological properties. Such modifications are known in the art and include those which increase biological penetration into a given biological system (e.g., blood, lymphatic system, central nervous system), increase oral availability, increase solubility to allow administration by injection, alter metabolism and alter rate of excretion.

Pharmaceutical Compositions

The pharmaceutical compositions of the present invention comprise a therapeutically effective amount of a compound of the present invention formulated together with one or more pharmaceutically acceptable carriers. As used herein, the term “pharmaceutically acceptable carrier” means a non-toxic, inert solid, semi-solid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type. Some examples of materials which can serve as pharmaceutically acceptable carriers are sugars such as lactose, glucose and sucrose; starches such as corn starch and potato starch; cellulose and its derivatives such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients such as cocoa butter and suppository waxes; oils such as peanut oil, cottonseed oil; safflower oil; sesame oil; olive oil; corn oil and soybean oil; glycols; such a propylene glycol; esters such as ethyl oleate and ethyl laurate; agar; buffering agents such as magnesium hydroxide and aluminum hydroxide; alginic acid; pyrogen-free water; isotonic saline; Ringer's solution; ethyl alcohol, and phosphate buffer solutions, as well as other non-toxic compatible lubricants such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, releasing agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the composition, according to the judgment of the formulator. The pharmaceutical compositions of this invention can be administered to humans and other animals orally, rectally, parenterally, intracisternally, intravaginally, intraperitoneally, topically (as by powders, ointments, or drops), buccally, or as an oral or nasal spray.

Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs. In addition to the active compounds, the liquid dosage forms may contain inert diluents commonly used in the art such as, for example, water or other solvents, solubilizing agents and emulsifiers such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, dimethylformamide, oils (in particular, cottonseed, groundnut, corn, germ, olive, castor, and sesame oils), glycerol, tetrahydrofurfuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, and mixtures thereof. Besides inert diluents, the oral compositions can also include adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, and perfuming agents.

Injectable preparations, for example, sterile injectable aqueous or oleaginous suspensions may be formulated according to the known art using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution, suspension or emulsion in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution, U.S.P. and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil can be employed including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid are used in the preparation of injectables.

The injectable formulations can be sterilized, for example, by filtration through a bacterial-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can be dissolved or dispersed in sterile water or other sterile injectable medium prior to use.

In order to prolong the effect of a drug, it is often desirable to slow the absorption of the drug from subcutaneous or intramuscular injection. This may be accomplished by the use of a liquid suspension of crystalline or amorphous material with poor water solubility. The rate of absorption of the drug then depends upon its rate of dissolution which, in turn, may depend upon crystal size and crystalline form. Alternatively, delayed absorption of a parenterally administered drug form is accomplished by dissolving or suspending the drug in an oil vehicle. Injectable depot forms are made by forming microencapsule matrices of the drug in biodegradable polymers such as polylactide-polyglycolide. Depending upon the ratio of drug to polymer and the nature of the particular polymer employed, the rate of drug release can be controlled. Examples of other biodegradable polymers include poly(orthoesters) and poly(anhydrides). Depot injectable formulations are also prepared by entrapping the drug in liposomes or microemulsions which are compatible with body tissues.

Compositions for rectal or vaginal administration are preferably suppositories which can be prepared by mixing the compounds of this invention with suitable non-irritating excipients or carriers such as cocoa butter, polyethylene glycol or a suppository wax which are solid at ambient temperature but liquid at body temperature and therefore melt in the rectum or vaginal cavity and release the active compound.

Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the active compound is mixed with at least one inert, pharmaceutically acceptable excipient or carrier such as sodium citrate or dicalcium phosphate and/or: a) fillers or extenders such as starches, lactose, sucrose, glucose, mannitol, and silicic acid, b) binders such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinylpyrrolidinone, sucrose, and acacia, c) humectants such as glycerol, d) disintegrating agents such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate, e) solution retarding agents such as paraffin, f) absorption accelerators such as quaternary ammonium compounds, g) wetting agents such as, for example, cetyl alcohol and glycerol monostearate, h) absorbents such as kaolin and bentonite clay, and i) lubricants such as talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, and mixtures thereof. In the case of capsules, tablets and pills, the dosage form may also comprise buffering agents.

Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like.

The active compounds can also be in micro-encapsulated form with one or more excipients as noted above. The solid dosage forms of tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells such as enteric coatings, release controlling coatings and other coatings well known in the pharmaceutical formulating art. In such solid dosage forms the active compound may be admixed with at least one inert diluent such as sucrose, lactose or starch. Such dosage forms may also comprise, as is normal practice, additional substances other than inert diluents, e.g., tableting lubricants and other tableting aids such a magnesium stearate and microcrystalline cellulose. In the case of capsules, tablets and pills, the dosage forms may also comprise buffering agents. They may optionally contain opacifying agents and can also be of a composition that they release the active ingredient(s) only, or preferentially, in a certain part of the intestinal tract, optionally, in a delayed manner. Examples of embedding compositions which can be used include polymeric substances and waxes.

Dosage forms for topical or transdermal administration of a compound of this invention include ointments, pastes, creams, lotions, gels, powders, solutions, sprays, inhalants or patches. The active component is admixed under sterile conditions with a pharmaceutically acceptable carrier and any needed preservatives or buffers as may be required. Ophthalmic formulation, ear drops, eye ointments, powders and solutions are also contemplated as being within the scope of this invention.

The ointments, pastes, creams and gels may contain, in addition to an active compound of this invention, excipients such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.

Powders and sprays can contain, in addition to the compounds of this invention, excipients such as lactose, talc, silicic acid, aluminum hydroxide, calcium silicates and polyamide powder, or mixtures of these substances. Sprays can additionally contain customary propellants such as chlorofluorohydrocarbons.

Transdermal patches have the added advantage of providing controlled delivery of a compound to the body. Such dosage forms can be made by dissolving or dispensing the compound in the proper medium. Absorption enhancers can also be used to increase the flux of the compound across the skin. The rate can be controlled by either providing a rate controlling membrane or by dispersing the compound in a polymer matrix or gel.

It will be understood, however, that the total daily usage of the compounds and compositions of the present invention will be decided by the attending physician within the scope of sound medical judgment. The specific therapeutically effective dose level for any particular patient will depend upon a variety of factors including the disorder being treated and the severity of the disorder; the activity of the specific compound employed; the specific composition employed; the age, body weight, general health, sex and diet of the patient; the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or contemporaneously with the specific compound employed; and like factors well known in the medical arts.

The total daily dose of the compounds of this invention administered to a human or other animal in single or in divided doses can be in amounts, for example, from 0.01 to 50 mg/kg body weight or more usually from 0.1 to 25 mg/kg body weight. Single dose compositions may contain such amounts or submultiples thereof to make up the daily dose. In general, treatment regimens according to the present invention comprise administration to a patient in need of such treatment from about 10 mg to about 1000 mg of the compound(s) of this invention per day in single or multiple doses.

Lower or higher doses than those recited above may be required. Specific dosage and treatment regimens for any particular patient will depend upon a variety of factors, including the activity of the specific compound employed, the age, body weight, general health status, sex, diet, time of administration, rate of excretion, drug combination, the severity and course of the disease, condition or symptoms, the patient's disposition to the disease, condition or symptoms, and the judgment of the treating physician.

Antiviral Activity

An inhibitory amount or dose of the compounds of the present invention may range from about 0.1 mg/Kg to about 500 mg/Kg, alternatively from about 1 to about 50 mg/Kg. Inhibitory amounts or doses will also vary depending on route of administration, as well as the possibility of co-usage with other agents.

According to the methods of treatment of the present invention, viral infections are treated or prevented in a subject such as a human or lower mammal by administering to the subject an anti-hepatitis C virally effective amount or an inhibitory amount of a compound of the present invention, in such amounts and for such time as is necessary to achieve the desired result. An additional method of the present invention is the treatment of biological samples with an inhibitory amount of a compound of composition of the present invention in such amounts and for such time as is necessary to achieve the desired result.

The term “anti-hepatitis C virally effective amount” of a compound of the invention, as used herein, mean a sufficient amount of the compound so as to decrease the viral load in a biological sample or in a subject. As well understood in the medical arts, an anti-hepatitis C virally effective amount of a compound of this invention will be at a reasonable benefit/risk ratio applicable to any medical treatment.

The term “inhibitory amount” of a compound of the present invention means a sufficient amount to decrease the hepatitis C viral load in a biological sample or a subject. It is understood that when said inhibitory amount of a compound of the present invention is administered to a subject it will be at a reasonable benefit/risk ratio applicable to any medical treatment as determined by a physician. The term “biological sample(s),” as used herein, means a substance of biological origin intended for administration to a subject. Examples of biological samples include, but are not limited to, blood and components thereof such as plasma, platelets, subpopulations of blood cells and the like; organs such as kidney, liver, heart, lung, and the like; sperm and ova; bone marrow and components thereof, or stem cells. Thus, another embodiment of the present invention is a method of treating a biological sample by contacting said biological sample with an inhibitory amount of a compound or pharmaceutical composition of the present invention.

Upon improvement of a subject's condition, a maintenance dose of a compound, composition or combination of this invention may be administered, if necessary. Subsequently, the dosage or frequency of administration, or both, may be reduced, as a function of the symptoms, to a level at which the improved condition is retained when the symptoms have been alleviated to the desired level, treatment should cease. The subject may, however, require intermittent treatment on a long-term basis upon any recurrence of disease symptoms.

An additional method of the present invention is the treatment of biological samples with an inhibitory amount of a compound of the present invention in such amounts and for such time as is necessary to inhibit viral replication and/or reduce viral load. The term “inhibitory amount” means a sufficient amount to inhibit viral replication and/or decrease the hepatitis C viral load in a biological sample. The term “biological sample(s)” as used herein means a substance of biological origin intended for administration to a subject. Examples of biological samples include, but are not limited to blood and components thereof such as plasma, platelets, subpopulations of blood cells and the like; organs such as kidney, liver, heart, lung, and the like; sperm and ova; bone marrow and components thereof; or stem cells. Thus another embodiment of the present invention is a method of treating a biological sample by contacting said biological sample with an inhibitory amount of a compound or pharmaceutical composition of the present invention.

Unless otherwise defined, all technical and scientific terms used herein are accorded the meaning commonly known to one with ordinary skill in the art. All publications, patents, published patent applications, and other references mentioned herein are hereby incorporated by reference in their entirety.

Abbreviations

Abbreviations which have been used in the descriptions of the schemes and the examples that follow are: <ul><li id="ul0023-0001" num="0189">ACN for acetonitrile;</li><li id="ul0023-0002" num="0190">BME for 2-mercaptoethanol;</li><li id="ul0023-0003" num="0191">BOP for benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate;</li><li id="ul0023-0004" num="0192">COD for cyclooctadiene;</li><li id="ul0023-0005" num="0193">DAST for diethylaminosulfur trifluoride;</li><li id="ul0023-0006" num="0194">DABCYL for 6-(N-4′-carboxy-4-(dimethylamino)azobenzene)-aminohexyl-1-O-(2-cyanoethyl)-(N,N-diisopropyl)-phosphoramidite;</li><li id="ul0023-0007" num="0195">DCM for dichloromethane;</li><li id="ul0023-0008" num="0196">DIAD for diisopropyl azodicarboxylate;</li><li id="ul0023-0009" num="0197">DIBAL-H for diisobutylaluminum hydride;</li><li id="ul0023-0010" num="0198">DIEA for diisopropyl ethylamine;</li><li id="ul0023-0011" num="0199">DMAP for N,N-dimethylaminopyridine;</li><li id="ul0023-0012" num="0200">DME for ethylene glycol dimethyl ether;</li><li id="ul0023-0013" num="0201">DMEM for Dulbecco's Modified Eagles Media;</li><li id="ul0023-0014" num="0202">DMF for N,N-dimethyl formamide;</li><li id="ul0023-0015" num="0203">DMSO for dimethylsulfoxide;</li><li id="ul0023-0016" num="0204">DUPHOS for</li></ul>

<chemistry id="CHEM-US-00346" num="00346"><img id="EMI-C00346" he="36.58mm" wi="29.04mm" file="US08809264-20140819-C00346.TIF" alt="embedded image" img-content="chem" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00346" attachment-type="cdx" file="US08809264-20140819-C00346.CDX" /><attachment idref="CHEM-US-00346" attachment-type="mol" file="US08809264-20140819-C00346.MOL" /></attachments></chemistry><ul><li id="ul0024-0001" num="0206">EDANS for 5-(2-Amino-ethylamino)-naphthalene-1-sulfonic acid;</li><li id="ul0024-0002" num="0207">EDCI or EDC for 1-(3-diethylaminopropyl)-3-ethylcarbodiimide hydrochloride;</li><li id="ul0024-0003" num="0208">EtOAc for ethyl acetate;</li><li id="ul0024-0004" num="0209">HATU for O (7-Azabenzotriazole-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate;</li><li id="ul0024-0005" num="0210">KHMDS is potassium bis(trimethylsilyl) amide;</li><li id="ul0024-0006" num="0211">Ms for mesyl;</li><li id="ul0024-0007" num="0212">NMM for N-4-methylmorpholine</li><li id="ul0024-0008" num="0213">PyBrOP for Bromo-tri-pyrrolidino-phosphonium hexafluorophosphate;</li><li id="ul0024-0009" num="0214">Ph for phenyl;</li><li id="ul0024-0010" num="0215">RCM for ring-closing metathesis;</li><li id="ul0024-0011" num="0216">RT for reverse transcription;</li><li id="ul0024-0012" num="0217">RT-PCR for reverse transcription-polymerase chain reaction;</li><li id="ul0024-0013" num="0218">TEA for triethyl amine;</li><li id="ul0024-0014" num="0219">TFA for trifluoroacetic acid;</li><li id="ul0024-0015" num="0220">THF for tetrahydrofuran;</li><li id="ul0024-0016" num="0221">TLC for thin layer chromatography;</li><li id="ul0024-0017" num="0222">TPP or PPh3 for triphenylphosphine;</li><li id="ul0024-0018" num="0223">tBOC or Boc for tert-butyloxy carbonyl; and</li><li id="ul0024-0019" num="0224">Xantphos for 4,5-Bis-diphenylphosphanyl-9,9-dimethyl-9H-xanthene.</li></ul>

Synthetic Methods

The compounds and processes of the present invention will be better understood in connection with the following synthetic schemes that illustrate the methods by which the compounds of the invention may be prepared.

All of the quinoxaline analogs were prepared from the common intermediate 1-6. The synthesis of compound 1-6 is outlined in Scheme 1. Deprotection of commercially available Boc-hydroxyproline 1-1 with HCl in dioxane followed by coupling with acid 1-2 using HATU, afforded intermediate 1-3. Other amino acid derivatives containing a terminal alkene may be used in place of 1-2 in order to generate varied macrocyclic structures (for further details see WO/0059929). Hydrolysis of 1-3 with LiOH followed by subsequent peptide coupling with cyclopropyl-containing amine 1-4 yielded tri-peptide 1-5. Finally, ring-closing metathesis with a ruthenium-based catalyst such as dichloro(o-isopropoxyphenylmethylene) (tricyclohexylphosphine)ruthenium(II) gave the desired key intermediate 1-6 (for further details on ring closing metathesis see recent reviews: Grubbs et al., Acc. Chem. Res., 1995, 28, 446; Shrock et al., Tetrahedron 1999, 55, 8141; Furstner, A. Angew. Chem. Int. Ed. 2000, 39, 3012; Trnka et al., Acc. Chem. Res. 2001, 34, 18; and Hoveyda et al., Chem. Eur. J. 2001, 7, 945).

The quinoxaline analogs of the present invention were prepared via several different synthetic routes. The simplest method, shown in Scheme 2, was to condense commercially available 1H-quinoxalin-2-one analogs including, but not limited to, compounds 2-2-2-5 with key intermediate 1-6 by using Mitsunobu conditions followed by hydrolysis with LiOH. The existing literature predicts Mistonobu product formation at the 1 position nitrogen, however attachment at the carbonyl oxygen was observed to form compound 2-1. A detailed discussion of the identification and characterization of the unexpected oxo Mitosunobu addition product appears in the examples herein. For further details on the Mitsunobu reaction, see O. Mitsunobu, Synthesis 1981, 1-28; D. L. Hughes, Org. React. 29, 1-162 (1983); D. L. Hughes, Organic Preparations and Procedures Int. 28, 127-164 (1996); and J. A. Dodge, S. A. Jones, Recent Res. Dev. Org. Chem. 1, 273-283 (1997).

Various quinoxaline derivatives of formula 3-3 can be made via the condensation of phenyl diamines of formula 3-1, wherein R6 is previously defined, with keto acids or esters of formula 3-2, wherein R7 is W—Z as previously defined, in anhydrous methanol at room temperature (see Bekerman et al., J. Heterocycl. Chem. 1992, 29, 129-133 for further details of this reaction). Examples of phenyl diamines suitable for creating quinoxaline derivatives of formula 3-3 include, but are not limited to, 1,2-diamino-4-nitrobenze, o-phenylenediamine, 3,4-diaminotoluene, 4-chloro-1,2-phenylenediamine, methyl-3,4-diaminobenzoate, benzo[1,3]dioxole-5,6-diamine, 1,2-diamino-4,5-methylene dioxybenzene, 4-chloro-5-(trifluoromethyl)-1,2-benzenediamine, and the like. Examples of keto acids suitable for the reaction described in Scheme 3 include, but are not limited to, benzoylformic acid, phenylpyruvic acid, indole-3-glyoxylic acid, indole-3-pyruvic acid, nitrophenylpyruvic acid, (2-furyl)glyoxylic acid, and the like. Examples of keto esters suitable for the reaction described in Scheme 3 include, but are not limited to ethyl thiophene-2-glyoxylate, ethyl 2-oxo-4-phenylbutyrate, ethyl 2-(formylamino)-4-thiazolyl glyoxylate, ethyl-2-amino-4-thiozolyl glyoxylate, ethyl-2-oxo-4-phenylbutyrate, ethyl-(5-bromothien-2-yl)glyoxylate, ethyl-3-indolylglyoxylate, ethyl-2-methylbenzoyl formate, ethyl-3-ethylbenzoyl formate, ethyl-3-ethylbenzoyl formate, ethyl-4-cyano-2-oxobutyrate, methyl(1-methylindolyl)-3-glyoxylate, and the like.

3,6-substituted quinoxalin-2-ones of formula 4-4, wherein R7 is W—Z as previously defined, can be made in a regioselective manner to favor the 6-position substitution beginning with the amide coupling of 4-methoxy-2-nitro aniline 4-1 and substituted glyoxylic acid 4-2 to yield compound 4-3. The 3,6-substituted quinoxalin-2-one 4-4 was created via catalytic reduction of the nitro of compound 4-3 followed by condensation. Other substituents may be introduced into 4-4 through the use of other 2-nitroanilines. Examples of keto acids suitable for the reaction described in Scheme 4 include, but are not limited to, benzoylformic acid, phenylpyruvic acid, indole-3-glyoxylic acid, indole-3-pyruvic acid, nitrophenylpyruvic acid, (2-furyl)glyoxylic acid, and the like. Examples of 2-nitro anilines suitable for the reaction described in Scheme 4 include, but are not limited to, 4-ethoxy-2-nitroaniline, 4-amino-3-nitrobenzotrifluoride, 4,5-dimethyl-2-nitroaniline, 4-fluoro-2-nitroaniline, 4-chloro-2-nitroaniline, 4-amino-3-nitromethylbenzoate, 4-benzoyl-2-nitroaniline, 3-bromo-4-methoxy-2-nitroaniline, 3′-amino-4′-methyl-2-nitroacetophenone, 5-ethoxy-4-fluoro-2-nitroaniline, 4-bromo-2-nitroaniline, 4-(trifluoromethoxy)-2-nitroaniline, ethyl-4-amino3-nitrobenzoate, 4-bromo-2-methyl-6-nitroaniline, 4-propoxy-2-nitroaniline, 5-(propylthio)-2-nitroaniline, and the like.

<chemistry id="CHEM-US-00351" num="00351"><img id="EMI-C00351" he="221.49mm" wi="76.20mm" file="US08809264-20140819-C00351.TIF" alt="embedded image" img-content="chem" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00351" attachment-type="cdx" file="US08809264-20140819-C00351.CDX" /><attachment idref="CHEM-US-00351" attachment-type="mol" file="US08809264-20140819-C00351.MOL" /></attachments></chemistry><chemistry id="CHEM-US-00352" num="00352"><img id="EMI-C00352" he="166.71mm" wi="72.98mm" file="US08809264-20140819-C00352.TIF" alt="embedded image" img-content="chem" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00352" attachment-type="cdx" file="US08809264-20140819-C00352.CDX" /><attachment idref="CHEM-US-00352" attachment-type="mol" file="US08809264-20140819-C00352.MOL" /></attachments></chemistry> A. A key intermediate, 3-chloro-1H-quinoxalin-2-one 5-3, can be synthesized in two steps beginning with the condensation of phenyl diamines of formula 3-1, as previously defined, and oxalic acid diethyl ester 5-1 under similar conditions as discussed in Scheme 3 (see Bekerman et al., J. Heterocycl. Chem. 1992, 29, 129-133). The resulting 1,4-dihydro-quinoxaline-2,3-dione 5-2 was then treated with SOCl2 (1.37 equiv.) in 1:40 DMF:toluene (see Loev et al, J. Med. Chem. (1985), 28, 363-366 for further details) to afford the desired intermediate 5-3. B. The key 3-chloro-quinoxalin-2-one 5-3 was added to the macrocyclic precursor 1-6 via Mitsunobu conditions, adding via the carbonyl oxygen rather than the expected 1-position nitrogen, to give the macrocylic intermediate of formula 5-4. This intermediate facilitates the introduction of various substituents at the 3-position of the quinoxaline. Suzuki Coupling

Compounds of formula 5-5, wherein R6 is previously defined and R is an aryl, substituted aryl, heteroaryl or substituted heteroaryl as previously defined, can be synthesized via Suzuki coupling reaction with an aryl, substituted aryl, heteroaryl, or substituted heteroaryl boronic acid in DME in the presence of Pd(PPh3)4, and CsCO3. For further details concerning the Suzuki coupling reaction see: A. Suzuki, Pure Appl. Chem. 1991, 63, 419-422 and A. R. Martin, Y. Yang, Acta Chem. Scand. 1993, 47, 221-230. Examples of boronic acids suitable for Suzuki coupling to macrocyclic key intermediate 5-5 include, but are not limited to, 2-bromo thiophene, phenylboronic acid, 5-bromothiophene-3-boronic acid, 4-cyanophenylboronic acid, 4-trifluormethoxyphenylboronic acid, and the like.

Sonogashira Reaction

Compounds of formula 5-6, wherein R1 is as previously defined and R6 is as previously defined, can be synthesized via Sonogashira reaction with the macrocyclic key intermediate and a terminal alkyne in acetonitrile in the presence triethylamine, PdCl2(PPh3)2, and CuI at 90° C. for 12 hours. For further details of the Sonogashira reaction see: Sonogashira, Comprehensive Organic Synthesis, Volume 3, Chapters 2, 4 and Sonogashira, Synthesis 1977, 777. Terminal alkenes suitable for the Sonogashira reaction with macrocyclic key intermediate 5-5 include, but are not limited to, ethynylbenzene, 4-cyano-ethynylbenzene, propargylbenzene, and the like.

Stille Coupling

Compounds of formula 5-7, wherein R6 is previously defined and R is an aryl, substituted aryl, heteroaryl or substituted heteroaryl as previously defined, can be synthesized via Stille coupling reaction with key macrocyclic intermediate of formula 5-4 and aryl stannanes in dioxane in the presence of Pd(PPh3)4. For further details of the Stille coupling reaction see: J. K. Stille, Angew. Chem. Int. Ed. 1986, 25, 508-524, M. Pereyre et al., Tin in Organic Synthesis (Butterworths, Boston, 1987) pp 185-207 passim, and a review of synthetic applications in T. N. Mitchell, Synthesis 1992, 803-815. Organostannanes suitable for Stille coupling with key macrocyclic intermediate 5-4 include, but are not limited to, tributyltin cyanide, allyl-tri-n-butyltin, 2-tributyltin-pyridine, 2-tri-n-butyltin furan, 2-tri-n-butyltin thiophene, 2,3-dihydron-5-(tri-n-butyltin)benzofuran, and the like.

Via the key macrocyclic 3-chloro-quinoxalinyl intermediate 5-4, three additional classes of substituents may be introduced at the 3-position of the quinoxaline ring. Among the various groups that may be introduced are mono-substituted amino, di-substituted amino, ethers, and thio-ethers.

The amino-substituted quinoxaline 6-1, wherein R4, R5, R6 are previously defined and R5 is Z as previously defined (see, e.g., Formula I), can be formed through adding K2CO3 (2.0 equiv.) and HNR4R5 (1.2 equiv.) to a 0.1M solution of macrocyclic quinoxalinyl intermediate 5-4 in 10 ml DMF, and stirring the resulting reaction mixture at room temperature for 5-12 hours. Amines suitable for these conditions include, but are not limited to, ethyl amine, 2-phenyl ethyl amine, cyclohexyl amine, ethylmethyl amine, diisopropyl amine, benzylethyl amine, 4-pentenyl amine, propargyl amine and the like.

For amines of the formula HNR4R5 wherein R4 is H and R5 is aryl, substituted aryl, heteroaryl, or substituted heteroaryl, a different set of conditions must be used to generate the corresponding compound 6-1. Addition of NaH (2.0 equiv.) and HNR4R5 (1.2 equiv.) to a 0.1M solution of the macrocyclic quinoxalinyl intermediate 5-4 in THF and stirring the resulting reaction mixture for 5-12 hours, afforded the aniline substituted compound 6-1. Amines suitable for these conditions are aniline, 4-methoxy aniline, 2-amino-pyridine, and the like.

Introduction of ethers to the 3-position of the quinoxaline ring can be achieved through treating a 0.1M solution of macrocyclic quinoxalinyl intermediate 5-4 in DMF with K2CO3 (2.0 equiv.) and HOR8 (1.2 equiv.), wherein R8═Z as previously defined. The resulting reaction mixture can then be stirred for 5-12 hours at room temperature to generate the desired ether moiety at the 3-position. Alcohols suitable for these conditions include, but are not limited to, ethanol, propanol, isobutanol, trifluoromethanol, phenol, 4-methoxyphenol, pyridin-3-ol, and the like. Thioesters can be made via the same procedure, e.g., by reaction of the macrocyclic quinoxalinyl intermediate 5-4 with a reagent of the form HS—R8.

Derivation of the benzo portion of the quinoxaline ring may be achieved through the halogen-substituted quinoxaline of formula 7-2. Quinoxaline of formula 7-2 can be formed via the condensation of bromo-substituted phenyldiamine 7-1 with a diketo compound of formula 3-2, wherein R7═W—Z as previously defined, in anhydrous methanol as previously detailed. Intermediate 7-3 was formed under Mitsunobu conditions with macrocyclic precursor 7-6 and bromosubstituted quinoxaline 7-2. Intermediate 7-3 may then undergo Suzuki coupling reactions, Sonogashira reactions, or Stille couplings at the position occupied by the bromo. See previous discussion of Suzuki couplings, Sonogashira reactions, and Stille couplings for further details. The Buchwald reaction allows for the substitution of amines, both primary and secondary, as well as 1H-nitrogen heterocycles at the aryl bromide. For further details of the Buchwald reaction see J. F. Hartwig, Angew. Chem. Int. Ed. 1998, 37, 2046-2067.

The 3-substituted 2-oxo-1,2-dihydro-quinoxaline-6-carboxylic acid intermediate 8-4 can be formed via condensation of ethyl 3,4-diaminobenzoate (8-1) with oxo acetic acid of formula 8-2, wherein R7═W—Z as previously defined, using the method described previously in Scheme 3 (see Bekerman et al., J. Heterocycl. Chem. 1992, 29, 129-133 for further details). The resulting ethyl ester 8-3 was then hydrolyzed with LiOH in MeOH at room temperature to yield carboxylic acid intermediate 8-4.

Carboxylic acid 8-4 then may be converted to substituted ketone 8-6 (wherein R1 is as previously defined) via Weinreb's amide 8-5 and subsequent treatment with various Grignard Reagents (see Weinreb et al. Tetrahedron Lett. 1977, 33, 4171; Weinreb et al, Synth. Commun. 1982, 12, 989 for details of the formation and use of Weinreb's amide; and see B. S. Furniss, A. J. Hannaford, P. W. G Smith, A. R. Tatchell, Vogel's Textbook of Practical Organic Chemistry, 5th ed., Longman, 1989). The addition was performed in an inert solvent, generally at low temperatures. Suitable solvents include, but are not limited to, tetrahydrofuran, diethylether, 1,4-dioxane, 1,2-dimethoxyethane, and hexanes. Preferably the solvent was tetrahydrofuran or diethylether. Preferably the reaction was carried out at −78° C. to 0° C.

Alternatively, carboxylic acid 8-4 may be used to form various amides of formula 8-7, wherein R4 is as previously defined, in a manner generally described in Scheme 8. All of the various quinoxalin-2-one compounds described in Scheme 8 are further coupled to the macrocyclic precursor via the Mitsunobu conditions described above.

Further 6-substituted quinoxalin-2-one compounds can be made via the general procedures set forth in Scheme 9.

A. Reduction of 6-nitro and Amide Formation

6-nitro-1H-quinoxalin-2-one (9-3) can be formed in the manner previously described from 3,4-diaminonitrobenzene and the oxo acetic acid of formula 9-2, wherein R7═W—Z as is previously described. Reduction of the nitro group at the 6-position can be achieved via Pd/C with H2NNH2.H2O in refluxing MeOH. The 6-position of amine 9-4 then can be treated with a wide array of acid chlorides to give various amides of formula 9-5 where R1 is as previously defined.

B. Oxidation of Benzyl Alcohol and Reductive Amination

Quinoxalin-2-one of formula 9-7 can be formed via the condensation of 3,4-diaminobenzyl alcohol and various oxo acetic acids of formula 9-2, wherein R7═W—Z as is previously described. The resulting benzyl alcohol 2-7 may then be oxidized under Swern conditions, or any other oxidation conditions, to generate aldehyde of formula 9-8. For further details concerning the Swern reaction see A. J. Mancuso, D. Swern, Synthesis 1981, 165-185 passim; T. T. Tidwell, Org. React. 1990, 39, 297-572 passim. For other oxidation conditions see B. S. Furniss, A. J. Hannaford, P. W. G Smith, A. R. Tatchell, Vogel's Textbook of Practical Organic Chemistry, 5th ed., Longman, 1989. Subsequent reductive amination reactions with primary or secondary amines in the presence of NaCNBH3 and acetic acid can yield compounds of formula 9-9 wherein R4 and R5 are as previously defined.

Hydrolysis of the preceding quinoxalinyl macrocyclic compounds was carried out in standard fashion. A solution of the ethyl ester 7-4 in THF/MeOH/H2O was treated with LiOH.H2O to directly afford the corresponding free acid wherein R6 is as previously defined and R7═W—Z as previously defined.

The sulfonamides 11-1 were prepared from the corresponding acids 10-1 by subjecting the acid to a coupling reagent (i.e. CDI, HATU, DCC, EDC and the like) at RT or at elevated temperature, with the subsequent addition of the corresponding sulfonamide R3—S(O)2—NH2 in the presence of base wherein R3, R6 and R are as previously defined and R7═W—Z as previously defined.

All references cited herein, whether in print, electronic, computer readable storage media or other form, are expressly incorporated by reference in their entirety, including but not limited to, abstracts, articles, journals, publications, texts, treatises, internet web sites, databases, patents, and patent publications.

Examples

The compounds and processes of the present invention will be better understood in connection with the following examples, which are intended as an illustration only and not to limit the scope of the invention. Various changes and modifications to the disclosed embodiments will be apparent to those skilled in the art and such changes and modifications including, without limitation, those relating to the chemical structures, substituents, derivatives, formulations and/or methods of the invention may be made without departing from the spirit of the invention and the scope of the appended claims

Example 1

Synthesis of the Cyclic Peptide Precursor

1A. To a solution of Boc-L-2-amino-8-nonenoic acid 1a (1.36 g, 5 mol) and the commercially available cis-L-hydroxyproline methyl ester 1b (1.09 g, 6 mmol) in 15 ml DMF, DIEA (4 ml, 4 eq.) and HATU (4 g, 2 eq) were added. The coupling was carried out at 0° C. over a period of 1 hour. The reaction mixture was diluted with 100 mL EtOAc, and directly washed with 5% citric acid (2×20 ml), water (2×20 ml), 1M NaHCO3 (4×20 ml) and brine (2×10 ml). The organic phase was dried over anhydrous Na2SO4, filtered, and then concentrated in vacuo, affording the dipeptide 1c (1.91 g, 95.8%) that was identified by HPLC (Retention time=8.9 min, 30-70%, 90% B), and MS (found 421.37, M+Na+).

1B. Dipeptide 1c (1.91 g) was dissolved in 15 mL of dioxane and 15 mL of 1 N LiOH aqueous solution, and the resulting mixture was stirred at room temperature for 4 hours. The reaction mixture was acidified by 5% citric acid and extracted with 100 mL EtOAc. The organic portion was then washed with water (2×20 ml), 1M NaHCO3 (2×20 ml) and brine (2×20 ml). The organic phase was dried over anhydrous Na2SO4, filtered, and then concentrated in vacuo, yielding the free carboxylic acid compound 1d (1.79 g, 97%), which was used directly without the need for further purification.

1C. To a solution of the free acid obtained above (1.77, 4.64 mmol) in 5 ml DMF, <smallcaps>D</smallcaps>-β-vinyl cyclopropane amino acid ethyl ester 1e (0.95 g, 5 mmol), DIEA (4 ml, 4 eq.) and HATU (4 g, 2 eq) were added. The coupling was carried out at 0° C. over a period of 5 hours. The reaction mixture was diluted with 80 mL EtOAc, and washed with 5% citric acid (2×20 ml), water (2×20 ml), 1M NaHCO3 (4×20 ml), and brine (2×10 ml). The organic phase was dried over anhydrous Na2SO4, filtered, and then concentrated in vacuo. The residue was purified by silica gel flash chromatography using gradient elution with hexanes:EtOAc (5:1→3:1→1:1→1:2→1:5). The linear tripeptide 1f was isolated as an oil (1.59 g, 65.4%) and identified by HPLC (Retention time=11.43 min) and MS (found 544.84, M+Na+).

1D. Ring Closing Metathesis (RCM). A solution of the linear tripeptide 1f (1.51 g, 2.89 mmol) in 200 ml dry DCM was deoxygenated by N2 bubbling. A catalyst for ring closing metathesis (RCM), (e.g., Grubbs' catalyst, Nolan's catalyst, or Hoveyda's catalyst, etc.) (e.g., 5 mol % eq.) was then added as a solid. The reaction was refluxed under N2 atmosphere for 12 hours. The solvent was evaporated and the residue was purified by silica gel flash chromatography using gradient elution with hexanes:EtOAc (9:1→5:1→3:1→1:1→1:2→1:5). The cyclic peptide precursor 1 was isolated as a white powder (1.24 g, 87%), and identified by HPLC (Retention time=7.84 min, 30-70%, 90% B), and MS (found 516.28, M+Na+). For further details of the synthetic methods employed to produce the cyclic peptide precursor 1, see WO 00/059929 (2000).

Example 2

Compound of Formula IV, wherein

Step 2A.

To a cooled mixture of macrocyclic precursor 1,3-(thiophen-2-yl)-1H-quinoxalin-2-one 2a (1.1 equiv.), and triphenylphosphine (2 equiv.) in THF was added DIAD (2 equiv.) dropwise at 0° C. The resulting mixture was held at 0° C. for 15 min. before being warmed to room temperature. After 18 hours, the mixture was concentrated under vacuum and the residue was purified by chromatography eluting with 60% EtOAc in hexanes to give 2b as a clear oil (35 mg, 99%).

MS (found): 704.4 (M+H).

H1-NMR [CDCl3, δ (ppm)]: 8.6 (d, 1H), 8.0 (d, 1H), 7.8 (d, 1H), 7.6 (m, 2H), 7.5 (d, 2H), 7.2 (t, 1H), 7.0 (brs, 1H), 6.0 (brt, 1H), 5.5 (m, 1H), 5.3 (brd, 1H), 5.2 (t, 1H), 5.0 (m. 1H), 4.6 (brt, 1H), 4.1-4.3 (m, 3H), 3.1 (m, 1H), 5.3 (m, 1H), 2.1-2.3 (m, 2H), 1.3 (brs, 9H), 1.2 (t, 3H).

Step 2B.

A solution of compound 2b and lithium hydroxide (10 equiv.) in THF/MeOH/H2O (2:1:0.5) was stirred at room temperature for 20 hours. The excess solvents were evaporated in vacuo, and the resulting residue was diluted with water and acidified to pH 5. The mixture was extracted with EtOAc (2×). The combined organic extracts were washed once with brine, dried (MgSO4), filtered and concentrated in vacuo to give an oily residue, which was purified by column chromatography eluting with 2-10% methanol-chloroform (87%).

MS (found): 676.3

1H-NMR [CD3OD, δ (ppm)]: 8.14 (1H), 7.96 (1H), 7.86 (1H), 7.65 (1H), 7.62 (1H), 7.59 (1H), 7.19 (1H), 6.07 (1H), 5.53 (1H), 5.52 (1H), 4.81 (1H), 4.75 (1H), 4.23 (1H), 4.12 (1H), 2.65-2.75 (2H), 2.52 (1H), 2.21 (1H), 1.97 (1H), 1.80 (1H), 1.62 (2H), 1.54 (1H), 1.47 (2H), 1.44 (2H), 1.41 (2H), 1.09 (9H).

13C-NMR [CD3OD, δ (ppm)]: 176.2, 174.1, 173.4, 156.0, 152.9, 141.0, 139.6, 138.9, 138.6, 131.5, 130.6, 130.0, 129.3, 128.1, 127.8, 127.1, 126.6, 78.6, 76.1, 59.8, 53.3, 52.3, 41.4, 34.5, 32.3, 30.0, 27.5, 27.4, 27.2 (3C), 26.1, 22.6, 22.4.

Example 3

Compound of Formula IV, wherein

Step 3A—Amine Deprotection.

The title compound of Step 2A (82 mg, 0.116 mmol) was treated with HCl (4 M in dioxane, 3 mL, 12 mmol). The reaction mixture was stirred at room temperature for 2 h until LCMS showed the complete consumption of starting material. The solvent was removed in vacuo.

Step 3B—Chloroformate Reagent

The chloroformate reagent 3b was prepared by dissolving 0.22 mmol of cyclopentanol in THF (5 ml) and adding 0.45 mmol of phosgene in toluene (20%). The resulting reaction mixture was stirred at room temperature for 2 hours and the solvent was removed in vacuo. To the residue was added DCM and subsequently concentrated to dryness twice in vacuo yielding chloroformate reagent 3b.

Step 3C—Carbamate Formation

The resulting residue from step 3a was dissolved in DCM (3 mL) then treated with cyclopentyl chloroformate prepared in step 3b (0.22 mmol) and iPr2NEt (0.35 mL, 2 mmol). The reaction mixture was stirred for 2.5 h. Ethyl acetate (15 mL) was added to the solution. The mixture was washed with saturated aqueous NaHCO3 solution, Water and brine consequently. The organic layer was dried over anhydrous sodium sulfate. The organic phase was then filtered, concentrated in vacuo and subsequently purified by flash chromatography (Ethyl acetate/hexanes 1:2) to give 60.0 mg of the ester. MS (ESI) m/z 716.31 (M+H)−.

Step 3D—Hydrolysis of the Ester

The ester from step 3c was hydrolyzed by the procedure set forth in Example 2 to give the title compound (42.0 mg 55% for 3 steps).

MS (ESI) m/z 688.37 (M+H)+.

13C-NMR (125 MHz, CD3OD): δ 174.6, 173.5, 173.0, 156.7, 152.9, 141.1, 140.0, 139.2, 138.8, 133.4, 130.8, 130.1, 129.3, 128.0, 127.2, 126.7, 126.3, 77.5, 76.2, 59.7, 53.3, 52.6, 40.3, 34.8, 34.4, 32.4, 32.2, 32.1, 30.8, 27.5, 27.4, 26.4, 23.6, 23.3, 23.0, 22.3.

Example 4

Compound of Formula IV, wherein

The title compound was prepared with the compound from step 2A in 4 ml of a 4M solution of HCl in dioxane and stirring the reaction mixture for 1 hour. The reaction residue was concentrated in vacuo. To this residue, 4 ml of THF and 0.045 mmol of TEA was added, the mixture was cooled to 0° C., to which was added 0.045 mmol of the cyclopentyl acid chloride. The resulting reaction mixture was stirred for 2 hours at 0° C. The reaction mixture was then extracted with EtOAc, washed with 1M sodium bicarbonate, water and brine, dried over MgSO4 and concentrated to dryness in vacuo. The crude compound was purified by silica column and the ethyl ester was subsequently hydrolyzed by the procedure set forth in Example 2.

Example 5

Compound of Formula IV, wherein

The title compound was prepared with the compound 2b in 4 ml of a 4M solution of HCl in dioxane and stirring for 1 hour. The resulting reaction residue was concentrated in vacuo, dissolved in 4 ml THF, and cooled to 0° C. To the 0° C. solution was added 0.045 mmol of cyclopentyl isocyanate and the resulting reaction mixture was stirred at room temperature for 4 hours. The solution was then extracted with EtOAc, washed with 1% HCl, water and brine, dried over MgSO4, and concentrated in vacuo to dryness. The crude compound was purified by silica column and the ethyl ester was subsequently hydrolyzed by the procedure set forth in Example 2.

Examples 6-14, Formula IV, where A=tBOC, are made by reacting the title compound of Example 1 with an appropriate 1H-quinoxalin-2-one

<chemistry id="CHEM-US-00370" num="00370"><img id="EMI-C00370" he="15.16mm" wi="36.49mm" file="US08809264-20140819-C00370.TIF" alt="embedded image" img-content="chem" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00370" attachment-type="cdx" file="US08809264-20140819-C00370.CDX" /><attachment idref="CHEM-US-00370" attachment-type="mol" file="US08809264-20140819-C00370.MOL" /></attachments></chemistry> under the Mitsunobu conditions described in Example 2, followed by the hydrolysis of the ethyl ester via treatment with LiOH as elucidated in Example 2. The 1H-quinoxalin-2-ones

<chemistry id="CHEM-US-00371" num="00371"><img id="EMI-C00371" he="15.16mm" wi="36.49mm" file="US08809264-20140819-C00371.TIF" alt="embedded image" img-content="chem" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00371" attachment-type="cdx" file="US08809264-20140819-C00371.CDX" /><attachment idref="CHEM-US-00371" attachment-type="mol" file="US08809264-20140819-C00371.MOL" /></attachments></chemistry> used in the examples are either commercially available or can be made from readily available starting materials via synthetic methods described in Schemes 3-9, or by synthetic methods well known by one with ordinary skill in the art.

Example 6

Compound of Formula IV, wherein

MS (ESI) m/z 736.18 (M+H)+.

Example 7

Compound of Formula IV, wherein

MS (ESI) m/z 710.22 (M+H)+.

Example 8

Compound of Formula IV, wherein

MS (ESI) m/z 697.4 (M+H)+.

Example 9

Compound of Formula IV, wherein A

MS (ESI) m/z 696.4 (M+H)+.

Example 10

Compound of Formula IV, wherein

MS (ESI) m/z 726.2 (M+H)+.

Example 11

Compound of Formula IV, wherein

MS (ESI) m/z 716.2 (M+H)+.

Example 12

Compound of Formula IV, wherein

MS (ESI) m/z 703.1 (M+H)+.

Example 13

Compound of Formula IV, wherein

MS (ESI) m/z 702.0 (M+H)+.

Example 14

Compound of Formula IV, wherein

MS (ESI) m/z 705.50 (M+H)+.

Examples 15-25, Formula IV, where

<chemistry id="CHEM-US-00381" num="00381"><img id="EMI-C00381" he="15.32mm" wi="34.71mm" file="US08809264-20140819-C00381.TIF" alt="embedded image" img-content="chem" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00381" attachment-type="cdx" file="US08809264-20140819-C00381.CDX" /><attachment idref="CHEM-US-00381" attachment-type="mol" file="US08809264-20140819-C00381.MOL" /></attachments></chemistry> are made by reacting the title compound of Example 1 with a corresponding 1H-quinoxalin-2-one

<chemistry id="CHEM-US-00382" num="00382"><img id="EMI-C00382" he="15.16mm" wi="36.49mm" file="US08809264-20140819-C00382.TIF" alt="embedded image" img-content="chem" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00382" attachment-type="cdx" file="US08809264-20140819-C00382.CDX" /><attachment idref="CHEM-US-00382" attachment-type="mol" file="US08809264-20140819-C00382.MOL" /></attachments></chemistry> under the Mitsunobu conditions described in step 2A, then followed by the procedures described in Example 3.

Example 15

Compound of Formula IV, wherein

MS (ESI) m/z 748.30 (M+H)+.

Example 16

Compound of Formula IV, wherein

MS (ESI) m/z 756.10 (M+H)+

Example 17

Compound of Formula IV, wherein

MS (ESI) m/z 718.11 (M+H)+.

Example 18

Compound of Formula IV, wherein

MS (ESI) m/z 718.11 (M+H)+.

Example 19

Compound of Formula IV, wherein

MS (ESI) m/z 748.20 (M+H)+

Example 20

Compound of Formula IV, wherein

MS (ESI) m/z 714.26 (M+H)+.

Example 21

Compound of Formula IV, wherein

MS (ESI) m/z 766.15 (M+H)+.

Example 22

Compound of Formula IV, wherein

MS (ESI) m/z 722.2 (M+H)+.

Example 23

Compound of Formula IV, wherein

MS (ESI) m/z 717.24 (M+H)+.

Example 24

Compound of Formula IV, wherein

MS (ESI) m/z 734.17 (M+H)+.

Example 25

Compound of Formula IV, wherein

MS (ESI) m/z 716.30 (M+H)+.

Examples 26-28 are made following the procedures described in Example 3 by using appropriate chloroformate reagents.

Example 26

Compound of Formula IV, wherein

MS (ESI) m/z 666.29 (M+H)+.

Example 27

Compound of Formula IV, wherein

MS (ESI) m/z 674.19 (M+H)+.

Example 28

Compound of Formula IV, wherein

MS (ESI) m/z 702.27 (M+H)+.

Examples 29-39 are made following the procedures described in Example 4 by using the corresponding activated acid derivatives:

Example 29

Compound of Formula IV, wherein

MS (ESI) m/z 686.28 (M+H)+.

Example 30

Compound of Formula IV, wherein

MS (ESI) m/z 680.35 (M+H)+.

Example 31

Compound of Formula IV, wherein

MS (ESI) m/z 669.35 (M+H)+.

Example 32

Compound of Formula IV, wherein

MS (ESI) m/z 683.37 (M+H)+.

Example 33

Compound of Formula IV, wherein

MS (ESI) m/z 670.33 (M+H)+.

Example 34

Compound of Formula IV, wherein

MS (ESI) m/z 697.37 (M+H)+.

Example 35

Compound of Formula IV, wherein

MS (ESI) m/z 712.39 (M+H)+.

Example 36

Compound of Formula IV, wherein

MS (ESI) m/z 670.34 (M+H)+.

Example 37

Compound of Formula IV, wherein

MS (ESI) m/z 670.31 (M+H)+.

Example 38

Compound of Formula IV, wherein

MS (ESI) m/z 670.09 (M+H)+.

Example 39

Compound of Formula IV, wherein

MS (ESI) m/z 712.38 (M+H)+.

Example 40

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 5.

MS (ESI) m/z 665.25 (M+H)+.

Example 41

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 2.

MS (ESI) m/z 682.08 (M+H)+.

Example 42

Compound of Formula IV, wherein

MS (ESI) m/z 670.33 (M+H)+.

Example 43

Compound of Formula IV, wherein

MS (ESI) m/z 698.41 (M+H)+.

Example 44

Compound of Formula IV, wherein

MS (ESI) m/z 685.43 (M+H)+.

Example 45

Compound of Formula IV, wherein

MS (ESI) m/z 722.14 (M+H)+.

Example 46

Compound of Formula IV, wherein

Step 46a: Cyclopropylsulfonyl chloride (1.4 g, 10 mmol) was dissolved in 0.5 M ammonia in dioxane (50 ml, 25 mmol) at RT. The reaction was kept at RT for 3 days. The large amount of precipitation was filtered and discarded. The clear filtrate was evaporated in vacuo and the white residue was dried on vacuum for 24 hours to give the cyclopropylsulfonamide (0.88 g, 74%). 1H-NMR (500 MHz, CD3Cl): δ 4.62 (2H, s), 2.59 (1H, m), 1.20 (2H, m), 1.02 (2H, m).

Step 46b: The title compound from Example 2 (21.0 mg, 0.031 mmol) and carbonyldiimidazole (6.0 mg, 0.037 mmol) were dissolved in 0.7 ml anhydrous DMF and the resulting solution was heated to 40° C. for 1 hour. Cyclopropylsulfonamide (8.0 mg, 0.06 mmol) was added to the reaction followed by DBU (7.0 mg, 0.046 mmol). The reaction mixture was stirred at 40° C. for 10 hour. LCMS showed the formation of the desired product. The reaction was cooled down and 10 ml ethyl acetate was added to the solution. The mixture was washed with saturated aqueous NaHCO3 solution, water and brine. The organic layer was dried over anhydrous sodium sulfate. The organic phase was then filtered, concentrated in vacuo and subsequently purified by flash chromatography (ethyl acetate/hexanes 1:1) to give 17.0 mg (71%) of the title compound.

MS (ESI) m/z 779.2 (M+H)+.

1H-NMR (500 MHz, CD3Cl): δ 10.24 (1H, s), 8.10 (1H, s), 8.00 (1H, d, J=8.0 Hz), 7.82 (1H, d, J=8.0 Hz), 7.60 (2H, m), 7.49 (1H, d, J=5.0 Hz), 7.16 (1H, s), 6.91 (1H, s), 6.09 (1H, s), 5.67 (1H, m), 5.12 (1H, m), 4.98 (1H, t, J=8.0 Hz), 4.70 (1H, t, J=8.0 Hz), 4.62 (2H, s), 4.33 (1H, m), 4.10 (1H, m), 2.92 (1H, m), 2.75 (2H, m), 2.58 (2H, m), 2.28 (1H, m), 1.91 (2H, m), 1.60-0.80 (20H, m).

13C-NMR (125 MHz, CD3Cl, 200-40 ppm region): δ 177.1, 173.5, 168.1, 155.2, 152.5, 140.7, 139.8, 139.1, 136.5, 130.5, 130.4, 129.7, 128.7, 128.3, 127.6, 127.1, 124.8, 80.1, 75.8, 59.7, 53.5, 52.3, 44.8.

Example 47

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 14.

MS (ESI): m/z 808.22 (M+H)+.

Example 48

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 3.

MS (ESI) m/z 791.2 (M+H)+.

1H-NMR (500 MHz, CD3Cl): δ 10.3 (1H, s), 8.10 (1H, d, J=3.5 Hz), 8.00 (1H, d, J=8.0 Hz), 7.83 (1H, d, J=8.0 Hz), 7.66-7.59 (2H, m), 7.48 (1H, d, J=5.0 Hz), 7.31 (1H, s), 7.14 (1H, t, J=4.2 Hz), 6.10 (1H, s), 5.60 (1H, m), 5.42 (1H, d, J=8.0 Hz), 4.92 (1H, t, J=8.0 Hz), 4.89 (3H, m), 4.71 (1H, t, J=8.0 Hz), 4.64 (1H, d, J=11.5 Hz), 4.39 (1H, m), 4.10 (1H, m), 2.88 (1H, m), 2.69 (2H, m), 2.58 (2H, m), 2.24 (1H, m), 1.95-0.80 (20H, m).

13C-NMR (125 MHz, CD3Cl): δ 177.4, 173.3, 168.4, 156.0, 152.5, 140.7, 140.0, 139.1, 136.5, 130.7, 130.3, 129.8, 128.7, 128.4, 127.6, 127.1, 124.7, 78.1, 75.9, 59.7, 53.5, 52.5, 44.7, 33.1, 32.7, 32.6, 31.3, 30.0, 27.5, 27.3, 26.3, 23.8, 22.4, 21.0, 6.9, 6.4, 6.3.

Example 49

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 23 and cyclopropylsulfonamide.

MS (ESI): m/z 820.22 (M+H)+.

Example 50

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the carboxylic acid from example 22 and cyclopropylsulfonamide.

MS (ESI) m/z 825.17 (M+H)+.

Example 51

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the carboxylic acid from example 19 and cyclopropylsulfonamide.

MS (ESI) m/z 851.33 (M+H)+.

Example 52

Compound of Formula IV, wherein

The title compound from Example 46 (164 mg, 0.21 mmol) was treated with HCl (4 M in dioxane, 3 mL, 12 mmol). The reaction mixture was stirred at room temperature for 0.5 h until LCMS showed the complete consumption of starting material. The solvent was removed in vacuo. CH2Cl2 (15 mL) was added then removed in vacuo (repeated 3 times) to give the title amine.

MS (ESI) m/z 679.36 (M+H)+.

Example 53

Compound of Formula IV, wherein

The title compound was prepared from the compound of Example 52 following the procedures described in Step 3b and Step 3c, by using cyclopent-3-enol.

MS (ESI) m/z 789.29 (M+H)+.

Example 54

Compound of Formula IV, wherein

The title compound was prepared from the compound of Example 52 following the procedures described in Step 3b and Step 3c, by using tetrahydro-pyran-4-ol.

MS (ESI) m/z 807.40 (M+H)+.

Example 55

Compound of Formula IV, wherein

The title compound was prepared from the compound of Example 52 following the procedures described in Step 3b and Step 3c, by using cyclobutanol.

MS (ESI) m/z 777.29 (M+H)+.

13C-NMR (125 MHz, CD3Cl): δ 177.3, 173.4, 168.4, 155.4, 152.5, 140.7, 139.7, 139.1, 136.5, 130.7, 130.3, 129.8, 128.7, 128.3, 127.7, 127.1, 124.7, 110.0, 75.7, 69.4, 59.8, 53.6, 52.5, 44.7, 34.9, 33.0, 31.3, 30.8, 30.2, 29.9, 27.4, 27.3, 26.3, 22.4, 14.4, 13.3, 6.9, 6.4.

Example 56

Compound of Formula IV, wherein

The title compound was prepared from the compound of Example 52 following the procedures described in Step 3b and Step 3c, by using methyl 1-hydroxycyclopropanecarboxylate.

MS (ESI) m/z 821.13 (M+H)+.

Example 57

Compound of Formula IV, wherein

The title compound was prepared from the compound of Example 52 following the procedures described in Example 4.

MS (ESI) m/z 789.15 (M+H)−.

Example 58

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 17 and cyclopropylsulfonamide.

MS (ESI): m/z 821.43 (M+H)+.

Example 59

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 18 and cyclopropylsulfonamide.

MS (ESI): m/z 821.44 (M+H)+.

Example 60

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 20 and cyclopropylsulfonamide.

MS (ESI): m/z 817.44 (M+H)+.

Example 61

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 45 and cyclopropylsulfonamide.

MS (ESI): m/z 825.32 (M+H)+.

Example 62

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 24 and cyclopropylsulfonamide.

MS (ESI): m/z 837.40 (M+H)+.

Example 63

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 42 and cyclopropylsulfonamide.

MS (ESI): m/z 773.54 (M+H)+.

Example 64

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 3 starting with the title compound of Example 63.

MS (ESI): m/z 785.40 (M+H)+.

Example 65

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 43 and cyclopropylsulfonamide.

MS (ESI): m/z 801.46 (M+H)+.

Example 66

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 3 by starting with the title compound of Example 65.

MS (ESI): m/z 813.52 (M+H)+.

Example 67

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 25 and cyclopropylsulfonamide.

MS (ESI): m/z 819.45 (M+H)+.

Example 68

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 44 and cyclopropylsulfonamide.

MS (ESI): m/z 788.48 (M+H)+.

Example 69

Compound of Formula IV, wherein

The title compound was prepared by treating the compound from Example 52 with 3,3-Dimethyl-butyraldehyde and NaBH3CN in acetonitrile.

MS (ESI): m/z 763.41 (M+H)+.

Example 70

Compound of Formula IV, wherein

The title compound was prepared by treating the compound from Example 46 with Iodomethane, K2CO3 in DMF.

MS (ESI): m/z 793.40 (M+H)+.

Example 71

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 3 and isopropylsulfonamide.

MS (ESI) m/z 793.5 (M+H)+.

Example 72

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 3 and 2,2,2-Trifluoro-ethanesulfonic acid amide.

MS (ESI) m/z 833.1 (M+H)+.

Example 73

Compound of Formula IV, wherein

The title compound was prepared following the procedure described in Example 46 by starting with the title compound of Example 3 and Trifluoro-methanesulfonamide.

MS (ESI) m/z 819.2 (M+H)+.

Example 74 to Example 111 (Formula IV) can be made following the procedures described in Examples 2, 3, 4, 5, 46, or 52.

<tables id="TABLE-US-00005" num="00005"><table frame="none" colsep="0" rowsep="0" pgwide="1"><tgroup align="left" colsep="0" rowsep="0" cols="2"><colspec colname="1" colwidth="343pt" align="center" /><colspec colname="2" colwidth="21pt" align="right" /><tbody valign="top"><row><entry namest="1" nameend="2" align="center" rowsep="1" /></row><row><entry /><entry>(IV)</entry></row><row><entry><chemistry id="CHEM-US-00443" num="00443"><img id="EMI-C00443" he="37.08mm" wi="48.60mm" file="US08809264-20140819-C00443.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment idref="CHEM-US-00443" attachment-type="cdx" file="US08809264-20140819-C00443.CDX" /><attachment idref="CHEM-US-00443" attachment-type="mol" file="US08809264-20140819-C00443.MOL" /></attachments></chemistry></entry><entry /></row><row><entry></entry></row></tbody></tgroup><tgroup align="left" colsep="0" rowsep="0" cols="4"><colspec colname="1" colwidth="35pt" align="center" /><colspec colname="2" colwidth="126pt" align="center" /><colspec colname="3" colwidth="126pt" align="center" /><colspec colname="4" colwidth="77pt" align="center" /><tbody valign="top"><row><entry>Example</entry><entry /><entry /><entry /></row><row><entry>#</entry><entry>A</entry><entry>Q</entry><entry>G</entry></row><row><entry namest="1" nameend="4" align="center" rowsep="1" /></row></tbody></tgroup><tgroup align="left" colsep="0" rowsep="0" cols="4"><colspec colname="1" colwidth="35pt" align="char" char="." /><colspec colname="2" colwidth="126pt" align="center" /><colspec colname="3" colwidth="126pt" align="center" /><colspec colname="4" colwidth="77pt" align="center" /><tbody valign="top"><row><entry>74</entry><entry><chemistry id="CHEM-US-00444" num="00444"><img id="EMI-C00444" he="15.32mm" wi="26.42mm" file="US08809264-20140819-C00444.TIF" alt="embedded image" img-content="table" img-format="tif" orientation="portrait" inline="no" /><attachments><attachment 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The compounds of the present invention exhibit potent inhibitory properties against the HCV NS3 protease. The following examples describe assays in which the compounds of the present invention can be tested for anti-HCV effects.

Example 112

NS3/NS4a Protease Enzyme Assay

HCV protease activity and inhibition is assayed using an internally quenched fluorogenic substrate. A DABCYL and an EDANS group are attached to opposite ends of a short peptide. Quenching of the EDANS fluorescence by the DABCYL group is relieved upon proteolytic cleavage. Fluorescence is measured with a Molecular Devices Fluoromax (or equivalent) using an excitation wavelength of 355 nm and an emission wavelength of 485 nm.

The assay is run in Corning white half-area 96-well plates (VWR 29444-312 [Corning 3693]) with full-length NS3 HCV protease 1b tethered with NS4A cofactor (final enzyme concentration 1 to 15 nM). The assay buffer is complemented with 10 μM NS4A cofactor Pep 4A (Anaspec 25336 or in-house, MW 1424.8). RET S1 (Ac-Asp-Glu-Asp(EDANS)-Glu-Glu-Abu-[COO]Ala-Ser-Lys-(DABCYL)-NH2, AnaSpec 22991, MW 1548.6) is used as the fluorogenic peptide substrate. The assay buffer contains 50 mM Hepes at pH 7.5, 30 mM NaCl and 10 mM BME. The enzyme reaction is followed over a 30 minutes time course at room temperature in the absence and presence of inhibitors.

The peptide inhibitors HCV Inh 1 (Anaspec 25345, MW 796.8) Ac-Asp-Glu-Met-Glu-Glu-Cys-OH, [−20° C.] and HCV Inh 2 (Anaspec 25346, MW 913.1) Ac-Asp-Glu-Dif-Cha-Cys-OH, are used as reference compounds.

IC50 values are calculated using XLFit in ActivityBase (IDBS) using equation 205: y=A+((B−A)/(1+((C/x)^D))).

Example 113

Cell-Based Replicon Assay

Quantification of HCV replicon RNA (HCV Cell Based Assay) is accomplished using the Huh 11-7 cell line (Lohmann, et al Science 285:110-113, 1999). Cells are seeded at 4×103 cells/well in 96 well plates and fed media containing DMEM (high glucose), 10% fetal calf serum, penicillin-streptomycin and non-essential amino acids. Cells are incubated in a 7.5% CO2 incubator at 37° C. At the end of the incubation period, total RNA is extracted and purified from cells using Ambion RNAqueous 96 Kit (Catalog No. AM1812). To amplify the HCV RNA so that sufficient material can be detected by an HCV specific probe (below), primers specific for HCV (below) mediate both the reverse transcription of the HCV RNA and the amplification of the cDNA by polymerase chain reaction (PCR) using the TaqMan One-Step RT-PCR Master Mix Kit (Applied Biosystems catalog no. 4309169). The nucleotide sequences of the RT-PCR primers, which are located in the NS5B region of the HCV genome, are the following:

<tables id="TABLE-US-00006" num="00006"><table frame="none" colsep="0" rowsep="0" tabstyle="monospace"><tgroup align="left" colsep="0" rowsep="0" cols="4"><colspec colname="offset" colwidth="14pt" align="left" /><colspec colname="1" colwidth="140pt" align="left" /><colspec colname="2" colwidth="63pt" align="left" /><colspec colname="3" colwidth="0pt" align="left" /><tbody valign="top"><row><entry /><entry>HCV Forward primer “RBNS5bfor”</entry><entry /><entry /></row><row><entry /><entry>5′GCTGCGGCCTGTCGAGCT:</entry><entry>(SEQ ID NO: 1)</entry></row><row><entry /><entry></entry></row><row><entry /><entry>HCV Reverse primer “RBNS5Brev”</entry></row><row><entry /><entry>5′CAAGGTCGTCTCCGCATAC.</entry><entry>(SEQ ID NO 2)</entry></row></tbody></tgroup></table></tables>

Detection of the RT-PCR product is accomplished using the Applied Biosystems (ABI) Prism 7500 Sequence Detection System (SDS) that detects the fluorescence that is emitted when the probe, which is labeled with a fluorescence reporter dye and a quencher dye, is degraded during the PCR reaction. The increase in the amount of fluorescence is measured during each cycle of PCR and reflects the increasing amount of RT-PCR product. Specifically, quantification is based on the threshold cycle, where the amplification plot crosses a defined fluorescence threshold. Comparison of the threshold cycles of the sample with a known standard provides a highly sensitive measure of relative template concentration in different samples (ABI User Bulletin #2 Dec. 11, 1997). The data is analyzed using the ABI SDS program version 1.7. The relative template concentration can be converted to RNA copy numbers by employing a standard curve of HCV RNA standards with known copy number (ABI User Bulletin #2 Dec. 11, 1997).

The RT-PCR product was detected using the following labeled probe:

<ul><li id="ul0025-0001" num="0556">5′ FAM-CGAAGCTCCAGGACTGCACGATGCT-TAMRA (SEQ ID NO: 3) FAM=Fluorescence reporter dye. TAMRA:=Quencher dye. </li></ul>

The RT reaction is performed at 48° C. for 30 minutes followed by PCR. Thermal cycler parameters used for the PCR reaction on the ABI Prism 7500 Sequence Detection System are: one cycle at 95° C., 10 minutes followed by 40 cycles each of which include one incubation at 95° C. for 15 seconds and a second incubation for 60° C. for 1 minute.

To normalize the data to an internal control molecule within the cellular RNA, RT-PCR is performed on the cellular messenger RNA glyceraldehyde-3-phosphate dehydrogenase (GAPDH). The GAPDH copy number is very stable in the cell lines used. GAPDH RT-PCR is performed on the same RNA sample from which the HCV copy number is determined. The GAPDH primers and probes are contained in the ABI Pre-Developed TaqMan Assay Kit (catalog no. 4310884E). The ratio of HCV/GAPDH RNA is used to calculate the activity of compounds evaluated for inhibition of HCV RNA replication.

Activity of Compounds as Inhibitors of HCV Replication (Cell Based Assay) in Replicon Containing Huh-7 Cell Lines.

The effect of a specific anti-viral compound on HCV replicon RNA levels in Huh-11-7 cells is determined by comparing the amount of HCV RNA normalized to GAPDH (e.g. the ratio of HCV/GAPDH) in the cells exposed to compound versus cells exposed to the DMSO vehicle (negative control). Specifically, cells are seeded at 4×103 cells/well in a 96 well plate and are incubated either with: 1) media containing 1% DMSO (0% inhibition control), or 2) media/1% DMSO containing a fixed concentration of compound. 96 well plates as described above are then incubated at 37° C. for 4 days (EC50 determination). Percent inhibition is defined as: % Inhibition=100−100*S/C1

where

S=the ratio of HCV RNA copy number/GAPDH RNA copy number in the sample;

C1=the ratio of HCV RNA copy number/GAPDH RNA copy number in the 0% inhibition control (media/1% DMSO).

The dose-response curve of the inhibitor is generated by adding compound in serial, three-fold dilutions over three logs to wells starting with the highest concentration of a specific compound at 1.5 uM and ending with the lowest concentration of 0.23 nM. Further dilution series (500 nM to 0.08 nM for example) is performed if the EC50 value is not positioned well on the curve. EC50 is determined with the IDBS Activity Base program “XL Fit” using a 4-paramater, non-linear regression fit (model #205 in version 4.2.1, build 16).

In the above assays, representative compounds of the present invention were found to have HCV replication inhibitory activity and HCV NS3 protease inhibitory activity. For instance, representative compounds of formula II, as depicted above, showed significant HCV replication inhibitory activity. These compounds were also effective in inhibiting HCV NS3 proteases of different HCV genotypes including genotypes 1, 2, 3 and 4. As a non-limiting example, representative compounds in the preferred examples of formula II showed EC50s in the range of from less than 0.2 nM to about 2 nM using cell-based replicon assays. Representative compounds of these preferred examples also inhibited HCV NS3 proteases of different HCV genotypes, such as genotypes 1a, 1b, 2a, 2b, and 4a, with IC50s in the range of from less than 0.2 nM to about 50 nM.

Representative compounds of the present invention were found to possess at least 10× improvements in potency as compared to their corresponding acid derivatives in the HCV NS3 protease inhibitory activity assay.

Pharmacokinetic analysis of representing compounds showed high liver drug levels. The concentration ratio of liver/plasma were found to be about 50 to 500 for these compounds.

Pharmacokinetic analysis of representing compounds showed high liver drug levels and low plasma and heart drug levels. For a single oral dose of 20 mg/kg in rat, compounds of formulae II′ and II″ showed a ratio of liver drug concentration/plasma concentration of ˜100 to ˜300 at 3 hours after dose. In addition, compound of formula II′ yielded concentrations in liver at 24 hours post dose that was 600-fold more than its replicon EC50 value. At 20 mg/kg in rat, compound of formula II′ also displayed less drug concentration in heart than in plasma with a Cmax ratio of drug concentration of heart/plasma at 0.15.

Compounds of the invention showed no significant inhibitions of Cytochrome P450 enzymes.

Although the invention has been described with respect to various preferred embodiments, it is not intended to be limited thereto, but rather those skilled in the art will recognize that variations and modifications may be made therein which are within the spirit of the invention and the scope of the appended claims.

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Every citation, both waysCites: the store holds 16 of 17

Citations
Document	Relation	Office	Cited during
WO03099274A1	Cites	World Intellectual Property Organization (WIPO)	Search report
WO2004037855A1	Cites	World Intellectual Property Organization (WIPO)	Applicant
WO2004072243A2	Cites	World Intellectual Property Organization (WIPO)	Applicant
WO2004093798A2	Cites	World Intellectual Property Organization (WIPO)	Applicant
US2004266668A1	Cites	United States of America	Applicant
WO2005028501A1	Cites	World Intellectual Property Organization (WIPO)	Applicant
WO2005070955A1	Cites	World Intellectual Property Organization (WIPO)	Applicant
US2005119168A1	Cites	United States of America	Search report
US2005153900A1	Cites	United States of America	Search report
US2005164921A1	Cites	United States of America	Search report
WO2007017144A2	Cites	World Intellectual Property Organization (WIPO)	Applicant
US2007060510A1	Cites	United States of America	Applicant
US2007099825A1	Cites	United States of America	Applicant
US6608027B1	Cites	United States of America	Applicant
US7173004B2	Cites	United States of America	Applicant
US7176208B2	Cites	United States of America	Applicant
H.-K. Han. AAPS Pharmsci. (2000) 2(1), article 6, pp. 1-11).	Non-patent	–	Search report
Ettmayer P. et al. J. Med. Chem. (2004) 47(10), pp. 2393-2404.	Non-patent	–	Search report
Tsantrizos et al, "Macrocyclic Inhibitors of the NS3 Protease as Potential Therapeutic Agents of Hepatitis C Virus Infection," Angew. Chem. Int. Ed. (2003), vol. 42, pp. 1356-1313.	Non-patent	–	Search report
U.S. Appl. No. 11/499,917, filed Aug. 4, 2006, Gai et al.	Non-patent	–	Applicant
U.S. Appl. No. 11/768,712, filed Jun. 26, 2007, Niu et al.	Non-patent	–	Applicant
R.C. Griffith et al., "HCV Anti-viral Agents", Annual Reports in Medicinal Chemistry, vol. 39, p. 223-237. (2004 Elsevier Inc.).	Non-patent	–	Applicant
Yan, et al., "Complex of NS3 Protease and NS4A Peptide of BK Strain Hepatitis C Virus: A 2.2 A Resolution Structure in a Hexagonal Crystal Form", Protein Science, vol. 7, p. 837-847.	Non-patent	–	Applicant

32 members in 18 offices

This recordMember, by publication datePriority claim8 more offices are in the list below

Priority claims6

Priority claims
Document	Office	Kind	Date
87244206	United States of America	P	2006-06-26
87244206	United States of America	P	2006-06-26
76872307	United States of America	A	2007-06-26
60872442	–	–	–
US20060872442P	–	–	–
US20070768723	–	–	–

Members32

Family members, oldest first
Document	Office	Kind
US2007299078A1	United States of America	A1	2007-12-27
AU2007265157A1	Australia	A1	2008-01-03
CA2654945A1	Canada	A1	2008-01-03
WO2008002924A2	World Intellectual Property Organization (WIPO)	A2	2008-01-03
US2008008681A1	United States of America	A1	2008-01-10
UY30437A1	Uruguay	A1	2008-01-31
TW200810777A	Taiwan Province of China	A	2008-03-01
WO2008002924A3	World Intellectual Property Organization (WIPO)	A3	2008-04-03
PE20080992A1	Peru	A1	2008-08-06
AR061629A1	Argentina	A1	2008-09-10
US2009005387A1	United States of America	A1	2009-01-01
KR20090023732A	Republic of Korea	A	2009-03-05
MX2008016528A	Mexico	A	2009-03-31
EP2066326A2	European Patent Office (EPO)	A2	2009-06-10
CN101478970A	China	A	2009-07-08
ZA200810519B	South Africa	B	2009-08-26
IL195512A0	Israel	A0	2009-09-01
JP2009541491A	Japan	A	2009-11-26
RU2009102252A	Russian Federation	A	2010-08-10
EP2066326A4	European Patent Office (EPO)	A4	2010-09-29
NZ573275A	New Zealand	A	2011-12-22
BRPI0714074A2	Brazil	A2	2012-12-18
RU2475494C2	Russian Federation	C2	2013-02-20
AU2007265157B2	Australia	B2	2013-06-27
CA2654945C	Canada	C	2013-08-06
US8501681B2	United States of America	B2	2013-08-06
IL195512A	Israel	A	2014-05-28
JP5520046B2	Japan	B2	2014-06-11
CN101478970B	China	B	2014-07-02
US8809264B2This record	United States of America	B2	2014-08-19
TWI454264B	Taiwan Province of China	B	2014-10-01
KR101505056B1	Republic of Korea	B1	2015-03-23

91 transactions on the USPTO file

Allowed after 3 non-final rejections, 1 final rejection, 2 RCEs and 2 appeals.

Non-final rejections: 3
Final rejections: 1
RCEs: 2
Appeals: 2

Over time

Point at a mark for the transaction

Transactions

Prosecution transactions, newest first
	Event	Code
2018-09-24	Expire PatentEXP.	EXP.
2018-04-02	Maintenance Fee Reminder MailedREM.	REM.
2015-10-21	Email NotificationEML_NTR	EML_NTR
2015-10-21	Change in Power of Attorney (May Include Associate POA)PA..	PA..
2015-10-20	Correspondence Address ChangeC.AD	C.AD
2014-08-20	Sequence Moved to Public DatabaseCRFA	CRFA
2014-08-19	Recordation of Patent Grant MailedPGM/	PGM/
2014-08-19	Patent Issue Date Used in PTA CalculationAllowedPTAC	PTAC
2014-07-31	Email NotificationEML_NTR	EML_NTR
2014-07-30	Issue Notification MailedAllowedWPIR	WPIR
2014-07-18	Dispatch to FDCD1935	D1935
2014-06-27	Email NotificationEML_NTR	EML_NTR
2014-06-27	Printer Rush- No mailingTCPB	TCPB
2014-06-27	Mailing Corrected Notice of AllowabilityMCNOA	MCNOA
2014-06-25	Application Is Considered Ready for IssuePILS	PILS
2014-06-22	Corrected Notice of AllowabilityCNOA	CNOA
2014-06-20	Email NotificationEML_NTR	EML_NTR
2014-06-20	Mail Miscellaneous Communication to ApplicantMM327	MM327
2014-06-18	Pubs Case Remand to TCPUBTC	PUBTC
2014-06-17	Issue Fee Payment VerifiedN084	N084
2014-06-17	Issue Fee Payment ReceivedIFEE	IFEE
2014-06-16	Miscellaneous Communication to Applicant - No Action CountM327	M327
2014-03-29	Sequence Forwarded to Pubs on TapeCRFT	CRFT
2014-03-25	Mail Post CardPST_CRD	PST_CRD
2014-03-17	Email NotificationEML_NTF	EML_NTF
2014-03-17	Mail Notice of AllowanceAllowedMN/=.	MN/=.
2014-03-10	Notice of Allowance Data Verification CompletedAllowedN/=.	N/=.
2014-03-10	Case Docketed to Examiner in GAUDOCK	DOCK
2014-01-21	Date Forwarded to ExaminerFWDX	FWDX
2014-01-21	Disposal for a RCE / CPA / R129AbandonedABN9	ABN9
2014-01-10	Request for Continued Examination (RCE)RCEX	RCEX
2014-01-10	Request for Extension of Time - GrantedXT/G	XT/G
2014-01-10	Workflow - Request for RCE - BeginBRCE	BRCE
2013-06-12	Notice of Appeal FiledN/AP	N/AP
2013-06-12	Request for Extension of Time - GrantedXT/G	XT/G
2012-12-12	Mail Final Rejection (PTOL - 326)Final rejectionMCTFR	MCTFR
2012-12-09	Final RejectionFinal rejectionCTFR	CTFR
2012-10-07	Date Forwarded to ExaminerFWDX	FWDX
2012-10-02	Response after Non-Final ActionA...	A...
2012-10-02	Request for Extension of Time - GrantedXT/G	XT/G
2012-04-02	Mail Non-Final RejectionNon-final rejectionMCTNF	MCTNF
2012-03-23	Non-Final RejectionNon-final rejectionCTNF	CTNF
2012-02-17	Information Disclosure Statement consideredIDSC	IDSC
2012-02-17	Electronic Information Disclosure StatementEIDS.	EIDS.
2012-02-17	Information Disclosure Statement (IDS) FiledWIDS	WIDS
2012-01-31	Date Forwarded to ExaminerFWDX	FWDX
2012-01-31	Disposal for a RCE / CPA / R129AbandonedABN9	ABN9
2012-01-30	Request for Continued Examination (RCE)RCEX	RCEX
2012-01-30	Request for Extension of Time - GrantedXT/G	XT/G
2012-01-30	Workflow - Request for RCE - BeginBRCE	BRCE
2011-08-05	Information Disclosure Statement consideredIDSC	IDSC
2011-08-05	Reference capture on IDSRCAP	RCAP
2011-08-05	Information Disclosure Statement (IDS) FiledM844	M844
2011-08-05	Information Disclosure Statement (IDS) FiledWIDS	WIDS
2011-07-29	Notice of Appeal FiledN/AP	N/AP
2011-07-29	Request for Extension of Time - GrantedXT/G	XT/G
2011-02-01	Mail Non-Final RejectionNon-final rejectionMCTNF	MCTNF
2011-01-31	Non-Final RejectionNon-final rejectionCTNF	CTNF
2010-12-23	Change in Power of Attorney (May Include Associate POA)PA..	PA..
2010-12-21	Correspondence Address ChangeC.AD	C.AD
2010-11-21	Date Forwarded to ExaminerFWDX	FWDX
2010-11-12	Response after Non-Final ActionA...	A...
2010-11-12	Request for Extension of Time - GrantedXT/G	XT/G
2010-05-20	Mail Non-Final RejectionNon-final rejectionMCTNF	MCTNF
2010-05-10	Non-Final RejectionNon-final rejectionCTNF	CTNF
2010-04-20	Date Forwarded to ExaminerFWDX	FWDX
2010-04-01	Response to Election / Restriction FiledELC.	ELC.
2010-04-01	Request for Extension of Time - GrantedXT/G	XT/G
2010-02-04	Mail Restriction RequirementMCTRS	MCTRS
2010-02-01	Restriction/Election RequirementCTRS	CTRS
2010-01-13	Case Docketed to Examiner in GAUDOCK	DOCK
2008-01-04	Information Disclosure Statement consideredIDSC	IDSC
2008-01-04	Reference capture on IDSRCAP	RCAP
2008-01-04	Information Disclosure Statement (IDS) FiledM844	M844
2008-01-04	Information Disclosure Statement (IDS) FiledWIDS	WIDS
2008-01-02	Case Docketed to Examiner in GAUDOCK	DOCK
2007-12-27	PG-Pub Issue NotificationPG-ISSUE	PG-ISSUE
2007-10-27	IFW TSS Processing by Tech Center CompleteTSSCOMP	TSSCOMP
2007-10-19	Application Dispatched from OIPEOIPE	OIPE
2007-09-19	Sent to Classification ContractorPGPC	PGPC
2007-09-19	Application Is Now CompleteCOMP	COMP
2007-09-14	CRF Is Good Technically / Entered into DatabaseCRFE	CRFE
2007-09-07	Payment of additional filing fee/PreexamFLFEE	FLFEE
2007-09-07	A set of symbols and procedures, provided to the PTO on a set of computer listings, that describe inSEQLIST	SEQLIST
2007-09-07	CRF Disk Has Been Received by Preexam / Group / PCTCRFL	CRFL
2007-09-07	A statement by one or more inventors satisfying the requirement under 35 USC 115, Oath of the ApplicOATHDECL	OATHDECL
2007-08-09	Notice Mailed--Application Incomplete--Filing Date AssignedINCD	INCD
2007-07-20	Cleared by L&R (LARS)L128	L128
2007-06-29	Referred to Level 2 (LARS) by OIPE CSRL198	L198
2007-06-28	IFW Scan & PACR Auto Security ReviewSCAN	SCAN
2007-06-26	Initial Exam Team nnIEXX	IEXX

6 legal events, as the office reported them to INPADOC

Over the term

Point at a mark for the event

Events

Legal events, newest first
	Event	Code
2018-10-16	Lapsed due to failure to pay maintenance feeLapsedFP	FP
2018-09-24	Lapse for failure to pay maintenance feesLapsedPATENT EXPIRED FOR FAILURE TO PAY MAINTENANCE FEES (ORIGINAL EVENT CODE: EXP.); ENTITY STATUS OF PATENT OWNER: LARGE ENTITYLAPS	LAPS
2018-09-24	Information on status: patent discontinuationPATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362STCH	STCH
2018-04-02	Fee payment procedureMAINTENANCE FEE REMINDER MAILED (ORIGINAL EVENT CODE: REM.)FEPP	FEPP
2007-08-30	AssignmentAS	AS
2007-08-30	AssignmentAS	AS

Quinoxalinyl macrocyclic hepatitis C virus serine protease inhibitors

Claim Score by NHIP

Abstract

Term

TECHNICAL FIELD

BACKGROUND OF THE INVENTION

SUMMARY OF THE INVENTION

DETAILED DESCRIPTION OF THE INVENTION

DEFINITIONS

Priority claims6

Members32

Over time

Transactions

Over the term

Events

Numbers

Titles

Patent term adjustment

Classification

Abstract

Term

RELATED APPLICATION

TECHNICAL FIELD

BACKGROUND OF THE INVENTION

SUMMARY OF THE INVENTION

DETAILED DESCRIPTION OF THE INVENTION

DEFINITIONS

Priority claims6

Members32

Over time

Transactions

Over the term

Events

Numbers

Titles

Patent term adjustment

Classification